Next Article in Journal
Potential of Natural Phenolic Compounds as Antimicrobial Agents against Multidrug-Resistant Staphylococcus aureus in Chicken Meat
Previous Article in Journal
Ubiquitin-Dependent and Independent Proteasomal Degradation in Host-Pathogen Interactions
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 28
Issue 18
10.3390/molecules28186741
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Recent Advances in the Synthesis of Aromatic Azo Compounds

by
Meng-Yun Zhao
,
Yue-Feng Tang
and
Guo-Zhi Han
*
College of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, China
*
Author to whom correspondence should be addressed.
Molecules 2023, 28(18), 6741; https://doi.org/10.3390/molecules28186741
Submission received: 31 July 2023 / Revised: 11 September 2023 / Accepted: 12 September 2023 / Published: 21 September 2023
Browse Figures
Review Reports Versions Notes

Abstract

:
Aromatic azo compounds have -N=N- double bonds as well as a larger π electron conjugation system, which endows aromatic azo compounds with wide applications in the fields of functional materials. The properties of aromatic azo compounds are closely related to the substituents on their aromatic rings. However, traditional synthesis methods, such as the coupling of diazo salts, have a significant limitation with respect to the structural design of aromatic azo compounds. Therefore, many scientists have devoted their efforts to developing new synthetic methods. Moreover, recent advances in the synthesis of aromatic azo compounds have led to improvements in the design and preparation of light-response materials at the molecular level. This review summarizes the important synthetic progress of aromatic azo compounds in recent years, with an emphasis on the pioneering contribution of functional nanomaterials to the field.

1. Introduction

Azo compounds usually refer to compounds containing -N=N- double bond, which can be divided into aryl azo compounds and alkyl azo compounds depending on the substituents on the -N=N- double bonds, as well as symmetrical and asymmetrical azo compounds from the point of view of structure. Azo compounds date back to 1859, and the high reactivity of -N=N- double bonds endow azo compounds with wide applications in many fields such as organic dyes, radical reaction initiators, and so on [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32]. On the other hand, azo compounds have cis and trans isomers, which can convert to each other under light irradiation or heating, as was discovered as early as 1937. The special property further promotes the pioneering role of azo compounds in the field of optical functional materials. Among azo compounds, aromatic azo compounds have a higher π electron conjugation system along with higher chemical stability and thermal stability. Moreover, the substituents on the aromatic ring have a direct impact on their properties, which promoted the design of functional photoresponsive materials at the molecular level [33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74]. As a result, the research and application of aromatic azo compounds have received great attention and undergone significant development in the past ten years, as shown in Figure 1.
Generally, there are two traditional methods for synthesizing aromatic azo compounds, as shown in Scheme 1: one is the coupling reaction of diazo compounds with electron-rich aromatics, which has a fast reaction rate and high yield—however, the substrate scope of the method is narrow, with a low safety factor; another method is the Mills reaction, which produces aromatic azo compounds from nitroso aromatic compounds and primary aromatic amines catalyzed by acetic acid. Therefore, the development of green and efficient methods for the synthesis of aromatic azo compounds is a significant concern in the chemical community. In this paper, we summarized the important synthetic progress of aromatic azo compounds in recent years, with an emphasis on the pioneering contribution of functional nanomaterials to the field.

2. Advances in the Synthesis of Aromatic Azo Compounds

2.1. Direct Oxidation of Aromatic Amines and Their Derivatives

The direct oxidation of aromatic amines to form aromatic azo compounds has been shown to be a green and promising method due to the wide availability of raw materials with rich and diverse structures, overcoming many shortcomings of traditional synthesis methods. For the oxidant in this strategy, oxygen is the most ideal choice for the green and atomic economy. However, oxygen molecules usually require activation via certain catalyst to participate in this reaction, which limits the direct utilization of oxygen in this process. In the past decade, transition metal compounds have entered people’s awareness due to their variable valence states and redox potentials. Furthermore, catalyst circulation can be achieved by the oxygen in the air. For example, Dutta et al. developed a facile, cost-effective method by which to synthesize diverse symmetrical and unsymmetrical aromatic azo compounds with inexpensive mesoporous manganese oxide materials as the catalyst and air as the terminal oxidant. Under the atmospheric condition, a variety of aniline derivatives underwent oxidative homo-coupling or cross-coupling to form corresponding azo compounds with moderate-to-excellent yields. Mild reaction conditions with good reusability endow the catalytic protocol with strong application prospects. Mechanism research indicated that air played a key role in the process, as shown in Figure 2 [75].
The extensive use of solvents in traditional organic chemicals is an important cause of environmental problems; therefore, developing solvent-free reactions has long been an attractive research direction. In our previous work, we report a new one-step direct synthesis of aromatic azo compounds from anilines under mild conditions. With the catalysis of copper acetate assisted by a small amount of palladium salt, rapid conversion of anilines to aromatic azo compounds can be observed under base-free and solvent-free conditions. In addition, the cross-coupling reaction based on this strategy also realized satisfactory yields. In this strategy, copper ions play a key role in the catalytic cycle via the auxiliary effect of palladium salt and oxygen, as shown in Figure 3 [76]. This method provides not only a new green route for the synthesis of symmetric and asymmetric aromatic azo compounds but also a strategy for exploring the catalytic applications of transition metal compounds.
Intramolecular diazotization reactions are often a challenge due to the issues of steric hindrance and angular tension. Maier et al. reported a new method for the synthesis of novel cyclic azo benzenes using diarylamine as the raw material, as shown in Figure 4. m-CPBA (Dichloromethane) was used as the oxidant and HOAc (Acetic acid)/DCM (Dichloromethane) as the mixed solvent [77]. The discovery of cyclic azobenzenes provides a novel photomolecular switch. Diarylamines with strong electron-withdrawing groups and electron-donating groups as feedstock reduce yields. Amino-substituted diarylamines require later derivatization in order to react. In addition, the electronic properties of substituent groups only had a weak effect on the yields of the product. The main disadvantages of this method are limited substrate selectivity and the possibility of generating multiple by-products during the reaction.
As mentioned above, for the strategy of the direct oxidation of aromatic amines to form aromatic azo compounds, the control of the oxidation degree is an important issue; that is, the catalytic oxidation of aniline usually produces by-products such as nitrobenzene, azobenzene, and azobenzene oxide, which are closely related to the performance of the catalyst. Shukla et al. developed a kind of Cu-CeO2 nanoparticle via a one-pot method; then, using H2O2 as the oxidant and acetonitrile as the solvent, direct oxidation of aniline to form aromatic azo compounds with high yields and selectivity was realized, as shown in Figure 5 [78]. Under the optimized conditions and with 3.8% Cu-CeO2 catalyst, 95% conversion of aniline with 92% selectivity of azo benzene was obtained. In particular, the amount of Cu and Ce present in the spent catalyst was found to be almost the same as that of the pristine catalyst, which confirmed the stability and heterogeneity of the catalyst.
Alkyl 2-phenylazocarboxylates are a kind of asymmetric azo compound which can play a key role in various organic reactions such as the catalytic Mitsunobu reaction. However, the conditions for the synthesis of alkyl 2-phenylazocarboxylates are always very harsh. Kim et al. reported a route for the preparation of alkyl ethyl 2-phenylazocarboxylate from the oxidation of ethyl 2-Phenylhydrazinecarboxylate catalyzed by CuCl and DMAP (4-dimethylaminopyridine) in the presence of air [79], and yields of up to 95% were obtained within three hours (Figure 6). Furthermore, one advantage of this method is its strong tolerance to solvents and chlorinated solvents such as chloroform, dichloroethane, and dichloromethane, showing overall excellent reactivity.
Trichloroisocyanic acid (TCCA) is an excellent oxidizing agent due to its stability, harmlessness, and ease of handling. Su et al. used trichloroisocyanuric acid as an oxidizing agent to oxidize phenylhydrazine compounds for the preparation of azo compounds [80]. Under the optimized conditions, the highest yield of 97% was obtained. The mechanistic diagram of this reaction is shown in Figure 7. In addition, the method easily realizes gram-scale synthesis with a less restrictive substrate range, except for that with large steric hindrance.
Although there has been significant progress in the synthesis of aromatic azo compounds, there are relatively few reports on the construction of heteroaromatic azo derivatives. Jiang et al. reported a new method for the synthesis of azo compounds via pyrazol-5-amine iodination using t-butyl hydroperoxide (TBHP) as the oxidizer and copper salt as the catalyst [81]. The single-electron transfer (SET) mechanism (through oxidation of the reaction) is shown in Figure 8. Intermolecular iodination and oxidation simultaneously form C-I and N-N bonds, followed by oxidative dehydrogenation to synthesize azopyrroles and iodo-substituted azopyrroles with a wide diversity in substituents. The radical initiator of TBHP was essential for this transformation. Furthermore, the selective formation of highly functionalized heteroaromatic azo compounds can be controlled by the catalytic system. The mild reaction conditions, selective modification of pyrrole skeleton, and high bond-forming efficiency (BFE) endow this strategy with high value. The drawback of low yield in the derivatization reaction needs to be optimized for practical applications.
Overall, the direct oxidation of aromatic amines to synthesize azo compounds has many advantages; however, sometimes, the presence of peroxidation leads to more by-products. Additionally, some oxidants are not suitable for large-scale applications.

2.2. Reductive Coupling of Aromatic Nitro Compound

An important source of aromatic amine is the reduction of aromatic nitro compounds. Therefore, starting from aromatic nitro compounds to synthesize aromatic azo compounds in one step will greatly improve the economy and environmental friendliness of reactions. In recent years, this synthesis strategy has attracted widespread attention from the scientific research community. Mondal et al. prepared a kind of AuNPs using a discrete a nanoscale organic cage (OC1R) as a template (Au@OC1R) [82]. The cage-immobilized AuNPs can act as heterogeneous photocatalyst for the selective reduction of nitroaromatics by 2-propanol to form the corresponding azo compounds with high yields at room temperature, as shown in Figure 9. After optimizing the synthesis conditions, the corresponding azo compounds could be selectively obtained, with 99% conversion under UV irradiation for 2 h in an inert atmosphere. In addition, no azo compounds were produced in the absence of AuNPs or only in the presence of OC1R, which indicated that the AuNPs is crucial for the reaction. Furthermore, the OC1R endows the catalyst with the advantages of easy separation and good compatibility of functional groups. The work lays an innovative foundation for the development of a new strategy for the synthesis of azo compounds.
Due to quantum size effects, Pd nanoclusters (PdNCs) with diameters less than 2 nm exhibit better catalytic properties than ordinary Pd nanoparticles. Generally, these ultra-small PdNCs must be complexed with specific ligands to maintain stable morphology. Yan et al. reported a tandem reduction strategy for the selective conversion of nitroaromatics to five types of products—aniline, hydroxylamine, azoxybenzenes, azo compounds, and hydrazine compounds—under mild conditions, as shown in Figure 10 [83]. First, Pd(OAc)2 was in situ reduced by NaBH4 to form ultra-fine PdNCs. These ultra-fine PdNCs were stabilized via surface-ligating with nitroaromatics and uniformly dispersed in the solvent. Then, the selective reduction of nitroarene was catalyzed by the ultra-fine PdNCs. Products with the electron-donating group and the electron-withdrawing group were also obtained with high yields. In addition, nitro fused aromatic compounds such as nitronaphthalene also adopt this protocol with strong results, i.e., a high yield of 80%, which was rarely reported before. However, the hydroxylamine generated in the reaction is easily oxidized, which may produce side reactions, and further optimization of the reaction conditions is needed to improve the selectivity of the reaction.
At present, new functional materials such as boron nitride (BN) are flourishing in the field of catalysis. Similar to graphene, hexagonal boron nitride (h-BN) is a two-dimensional layered material with low toxicity and thermal stability. For catalytic application, h-BN can provide a supported platform and more reactive sites for metal nanoparticles. Liu et al. synthesized a kind of Au nanoparticle loaded on h-BN nanoplates (Au/BN). The composite catalyst can selectively catalyze the conversion of nitrobenzene to azobenzene or hydrogenated azobenzene in the presence of IPA (i-propyl alcohol)/KOH under N2 or air atmosphere, as shown in Figure 11 [84]. In the process, h-BN inhibited the activation of oxygen, allowing the catalytic hydrogenation of nitrobenzene in air. On the other hand, KOH takes away the hydrogen atom from the isopropanol, subsequently producing acetone and an activated H donor on the Au/BN surface. Au nanoparticles are then bound to the H donor to form H-Au. The active species of H-Au played a key role in the subsequent reduction process. Meanwhile, the H atoms in H-Au can collide with each other to produce H2 during the reaction for the next cycle.
Although the catalytic activity of noble metal nanoparticles is often excellent, the high cost has hindered their large-scale use. Therefore, other relatively inexpensive transition metals catalysts have attracted great attention. Pahalagedara et al. reported a sea urchin-like Ni/graphene nanocomposite for the selective reduction by hydrazine of nitroaromatics with different substituents to the corresponding azo compounds, and the magnetic catalyst was easily recycled and reused. In addition to stabilizing and dispersing nanoparticles, graphene can improve the contact between the reactants and the catalyst surface by interacting with nitroaromatics through p-p stacking, thus increasing the reaction rate, as shown in Figure 12 [85]. In the reduction process, hydrazine was first oxidized to produce the electrons necessary for the reduction, along with nitrogen and water. Then, the nitrobenzene was reduced to nitrosobenzene, which was further reduced to N-phenylhydroxylamine. The nitrosobenzene and N-phenylhydroxylamine were finally condensed to form the main product of azoxybenzene and azoxybenzene.
Wang et al. prepared a kind of Fe and N co-doped mesoporous carbon (NMC-Fe) as an efficient heterogeneous catalyst for the reduction of nitroaromatics to azo compounds via hydrazine hydrate, as shown in Figure 13 [86]. Doped N and Fe occupied vacant and defective sites in carbon nanosheets, which resulted in a smaller specific surface area than undoped carbon catalysts. Though both Fe-doped (MC-Fe) and N-doped (NMC) carbon materials can catalyze the reduction of 1,2-bis(4-chlorophenyl) diazene oxide to form (E)-1,2-bis(4-chlorophenyl) diazene, the Fe and N co-doped strategy endowed the reaction with higher selectivity. Typically, iron-based catalyst involve a hydrogen transfer mechanism. Negatively charged hydride was adsorbed at the iron active center (the electron-withdrawing group). The formed complexes act as hydrogen transfer centers for the selective reduction of nitroaromatics to azo compounds. However, in the absence of Fe or N, only azoxybenzene was obtained.
Compared to other transition metals, Cu is cheaper and more available and easier to handle. Moran et al. reported efficient copper nanoparticles (Cu(0)NPs) for the catalysis of nitroaromatics with the controlled and selective transfer of hydrogenation to prepare azo compounds through different hydrogen sources, as shown in Figure 14 [87]. The highlight of this work was that different hydrogen donors gave different products. For example, using ethanolamine as the hydrogen source, azo benzene was obtained with 96% selectivity after 25 h at 55 °C, and study of the substrate’s scope provided azo derivatives, with an average yield of 85%. However, using glycerol as the source of hydrogen, the end product was almost always aniline. Moreover, the nano-Cu material suppressed the rate of auto-oxidation, and only a trace of Cu2O was detected after 6 months, as well as the still-high catalytic activity.
As a hydrogen source for reduction reactions, hydrogen is undoubtedly a green and low-cost choice for industrialization. Hu et al. reported the preparation of the azo compounds from nitroaromatics under mild conditions catalyzed by a worm-like Pd nanomaterial. The diameter of the Pd catalyst was about 3.5 nm with a narrow size distribution. The worm-like Pd nanomaterial can catalyze the reduction of nitrobenzene to form azo-benzene via H2 in the presence of a base, whereas it forms aniline in the absence of a base. It is worth mentioning that higher yields were obtained for the electron-rich nitroaromatic compounds. In addition, asymmetric azo compounds were facilely synthesized by this method, with good yields [88]. The plausible mechanism proposed by the authors is shown in Figure 15. First, hydrogen was adsorbed on the surface of the palladium nanoparticles and reduced nitrobenzene to form nitrosobenzene, which, in turn, rapidly converted to N-phenylhydroxylamine. Under acidic or neutral conditions, N-phenylhydroxylamine was further reduced to aniline. Under alkaline conditions, N-phenylhydroxylamine combined with nitrosobenzene to form N, N′-dihydroxy-diphenylhydrazine, which was then further reduced to azobenzene. Moreover, excessive reduction products of hydrazobenzene can be spontaneously oxidized to azobenzene in air.
Huang et al. prepared a kind of cobalt/nitrogen-doped carbon (IPAx) catalyst for the selective reduction of nitroaromatics to aniline or aromatic azo compounds by H2, which depends on the basicity of the reaction system [89]. Furthermore, recycling experiments showed that the Co-Nx catalyst had excellent reusability. The mechanism of this reaction is shown in Figure 16. Similar to the classical reduction of nitrobenzene, nitrobenzene was first hydrogenated to form nitrosobenzene, followed by transfer to N-phenylhydroxylamine and finally aniline. However, the hydrogenation pathway of nitrobenzene was changed under basic conditions. The activating energy of the condensation reaction between N-phenylhydroxylamine and nitrosobenzene was reduced, as was the pathway in which N-phenylhydroxylamine transfer to aniline was inhibited. Therefore, azoxybenzene was readily produced.
Compared to the direct oxidative coupling of aromatic amines, the synthesis of aromatic azo compounds, through the reduction coupling of aromatic nitro compounds, undoubtedly has higher efficiency. However, the catalysts involved often have high costs, which limits their practical application prospects.

2.3. Electrochemical Method

Organic electrochemical synthesis has become a practical and environmentally friendly synthesis method and is widely used in oxidation and reduction reactions. In electrochemical synthesis, electrodes act as acceptors or donors of electrons to avoid, to a certain extent, the use of some harmful and dangerous chemical oxidation and reduction reagents, as well as to reduce the generation of chemical waste and improve production safety. Therefore, the electrochemical synthesis of some fine organic chemicals has attracted great attention in recent years. Qiao et al. first prepared a Ni3Fe-MOF-OH material with surface hydroxylation. Then, using the material as electrodes, azobenzene was synthesized via cathodic reduction of nitrobenzene and anodic oxidation of aniline, as shown in Figure 17 [90]. Experimental results indicated that the bimetallic Ni3Fe-MOF-OH electrocatalyst showed excellent performance in N-N coupling. In the process, the surface hydroxylation of the electrodes promoted the adsorption of nitrobenzene and aniline and improved the reaction rate. On the other hand, the competitive hydrogen and oxygen evolution reactions were suppressed due to the adsorption of nitroarenes and anilines via surface hydroxyls of the electrocatalyst. Moreover, using TEMPO as the electron medium, gram-scale reactions were realized with high selectivity.
Gong et al. prepared a kind of N-doped carbon nanotube-supported Ni-Co alloy nanoparticle (NiCo@N-CNTs) via a simple reductive pyrolysis strategy for the electrochemical synthesis of azobenzene [91]. In the Ni–Co-alloy nanoparticles, CoNPs confined at the tip of N-doped CNTs (N-CNTs) showed excellent activity and thermal stability toward thermochemical selective hydrogenation of aldehyde, ketone, carboxyl, and nitro groups. It was found that when Ni-Co@N-CNTs acted as cathodes, 100% conversion with 99% selectivity of oxidized azobenzene were achieved. Furthermore, in order to improve the energy utilization efficiency, the authors designed a NiCo@N-CNTs||Ni(OH)2/NF dual electrode electrolyzer, as shown in Figure 18. Simultaneous cathodic reduction of nitrobenzene and anodic oxidation of 5-hydroxymethylfurfural were achieved, with high yields. This work provides a new idea for the design and fabrication of highly active, durable, and low-cost electrocatalysts for other electrocatalytic syntheses.
Zhang et al. reported a method for the cross-coupling reaction of aromatic nitro compounds to aromatic azo compounds via base-free electrochemistry using SmI2 as a catalyst, as shown in Figure 19 [92]. Under the optimized conditions, desired asymmetric azo compounds were synthesized, with 83% yield and 99% selectivity. In this strategy, the electron-donating groups exhibited better adaptability. Moreover, the samarium electrode was rarely consumed in the reaction process and can be reused more than 100 times. The preliminary mechanistic study suggested that the formation of azobenzene was accomplished by successive single-electron reductions. The key step was the reduction of nitro benzene to a radical anionic intermediate. The rapid dimerization of this intermediate to produce oxo azobenzene was followed by a single-electron transfer reduction to form the desired product mediated by SmIIX2.
Although electrochemistry has many advantages, there are still some issues that need to be addressed. For example, in the process of electrochemical reaction, the electron transfer between the electrode and the substrate is heterogeneous, which would lead to overpotential and make the functional group tolerance of the reaction worse.

2.4. Photocatalytic Method

Photocatalytic synthesis is an emerging method in the organic field, in which the catalyst utilizes light energy to promote organic reaction. Compared with traditional organic synthesis, it has the advantages of mild reaction conditions, fast reaction speed, high selectivity, and lower energy consumption. Zhou et al. reported that Pd nanoparticles loaded on mesoporous CdS (Pd@ CdS) can act as a highly active and selective photocatalyst in water under visible light irradiation [93]. The photocatalytic conversion of glucose to arabinose and nitrosobenzene to azobenzene could be carried out simultaneously, catalyzed by the composite catalyst with ideal selectivity, as shown in Figure 20. In this process, photoexcited electrons were transferred from mesoporous CdS to PdNPs, thus inhibiting the recombination of electron–hole pairs and providing the active site on Pd for the reduction of nitrosobenzene to azobenzene, while glucose was photo-oxidized by holes to arabinose through C1-C2 bond cleavage. Moreover, the formic acid generated by glucose oxidation was conducive to the hydrogenation reaction of nitrobenzene. On the other hand, nitrobenzene promotes the conversion of glucose by accepting photoexcited electrons and H+ generated from water cleavage and glucose reforming.
Wang et al. reported a kind of CQDs/ZnIn2S4 nanocomposite for the controlled hydrogenation of nitrobenzene under visible light. By simply adjusting the alkalinity and hydrogen source, azobenzene or azoxybenzene were selectively produced [94]. When triethanolamine was used as the hydrogen source, 76% aniline was obtained. However, after a large amount of base was added, azobenzene was mainly produced, as shown in Figure 21. When irradiated by visible light, ZnIn2S4 was excited to generate electrons and holes, and CQDs (carbon quantum dots) transfer photogenerated electrons away from ZnIn2S4. With the assistance of triethanolamine (TEOA) as the hydrogen source, the electron-rich CQDs promote the gradual hydrogenation of nitrobenzene to aniline. Meanwhile, TEOA also acts as an electron donor, which reacts with photogenerated holes in ZnIn2S4 to complete the whole photocatalytic cycle. The introduction of bases such as NaOH into the reaction system promotes the condensation of nitrosobenzene with N-phenylhydroxylamine to form azoxybenzene, which can be further hydrogenated to produce azobenzene. Despite many advantages, photocatalytic synthesis still faces challenges such as low quantum efficiency, low solar energy utilization, and insufficient catalyst recycling rate.
Overall, photocatalysis is one of the key technologies currently being developed, and the design and synthesis of core catalysts are the most important factors. Catalysts based on noble metals are clearly not suitable for the promotion and application of this technology.

2.5. Biochemical Methods

Entering the 21st century, humanity has been facing an unprecedented crisis of survival and development due to continuous depletion of fossil fuels and increasing environmental pollution. Therefore, the traditional chemical industry must undergo revolutionary transformation. Biochemistry is just one of the technologies needed for the sustainable development of society. In the field of organic synthesis, the core of biochemistry is to use enzymes to replace traditional industrial catalysts, to promote chemical reactions with high efficiency and selectivity, and simultaneously, to reduce energy consumption and environmental pollution. Sousa et al. reported the synthesis of azo compounds via the oxidative coupling of primary aromatic amines catalyzed by laccase under mild reaction conditions, as shown in Figure 22 [95]. The enzyme first promoted the aerobic oxidation of amine to form an unstable intermediate of amino cation radical, which subsequently underwent deprotonation to produce an amino neutral radical. Then, two free radicals were coupled to form HN-NH bonds, which were dehydrogenated to give the corresponding azo compounds. However, there is one drawback of this strategy that cannot be ignored: for substrates containing electron-withdrawing groups, unstable radical intermediates may be generated, which results in low yields.
Ethyl lactate is a biodegradable and environmentally friendly biomass-derived solvent which is completely degradable, having non-toxicity and low-corrosivity. Pariyar et al. used ethyl lactate as a solvent for the facile one-step synthesis of symmetrical and asymmetrical aromatic azo compounds from amines [96]. In the strategy, ethyl lactate was used as an effective mediator to synthesize azobenzene from aniline under catalyst-free conditions, as shown in Figure 23. The oxidation of aniline by potassium peroxomonosulfate (oxone) is possibly conducted via a free radical mechanism or electrophilic oxygen transfer, producing the unstable nitrosobenzene. Subsequently, another molecule of aniline attacks the nitrosobenzene, followed by dehydration to give trans-azobenzene. In the process, ethyl lactate acted as a biological enzyme. Furthermore, the amines with electron-donating groups gave higher yields than those with electron-withdrawing groups. The most important advantage of this method is the use of environmentally friendly solvents, which act as mimic enzymes. However, the mechanism has not been elucidated yet, and this method is currently not suitable for the synthesis of asymmetric azo compounds.

2.6. Nitrogen–Halogen Exchange

In recent years, construction of -N=N- bonds using hydrazine hydrate as an inorganic dinitrogen source has received much attention, being a direct and green pathway for the synthesis of aromatic azo compounds. Xie et al. reported a copper-catalyzed diarylation reaction of hydrazine with cyclic/linear diaryl iodonium salts, which converted inorganic hydrazine into organic nitrogen-containing compounds to obtain a series of azobenzene derivatives, as shown in Figure 24 [97]. In this strategy, phthalhydrazide (PHA) was first formed via the hydrazinolysis of phthalic anhydride. At the same time, the coordination of CuI with 2,2′-bipyridine yielded a kind of CuI-complex (Int-A). The next process has two possible pathways: (1) Int-A underwent ligand exchange with PHA, followed by an oxidative addition of cyclic diphenyliodonium triflate (2a) to produce Int-B and Int-D in sequence (pathway a); (2) Int-A undergoes direct oxidative addition with 2a to produce Int-C, followed by ligand exchange to form Int-D (pathway b). Next, reductive elimination of Int-A gives the monoaryl compound IM 1. A second oxidative addition of IM 1 with Int-A gives Int-E, prior to subsequent intramolecular ligand coupling to form Int-F. A second reductive elimination of Int-A releases compound IM 2, which then undergoes K2CO3-mediated deprotection and oxidation to give the azo compound and potassium phthalic acid.
N-aryl-N′-silyldiazenes are a kind of kinetically stable aryl nucleophilic reagent. Finck et al. synthesized a series of asymmetrical azobenzene derivatives via palladium-catalyzed C-N coupling reactions between N-aryl-N′-silyl diazenes and aryl halides, as shown in Figure 25 [98]. First, L2Pd0(I) underwent oxidative addition with X-Ar2 to produce aryl palladium(II) halide (II). Then, the intermediate II underwent σ-bond complexation with the N-aryl-N′-silyldiazenes to produce transition state III. Subsequently, transition state III released Me3Si-X to produce intermediate IV, which was finally reduced to give asymmetric aromatic aromatics as well as L2Pd0(I), thus completing the catalytic cycle. It is worth noting that the presence of the base is crucial, and Cs2CO3 was the optimized choice.
Overall, the strategy of nitrogen–halogen exchange has shown good application prospects in the construction of asymmetric aromatic azo compounds, but the tolerance of functional groups and product yields still need to be further improved.

3. Conclusions

Azo aromatic compounds are important functional molecules and chemical raw materials which are widely used in the fields of organic dyes, optical materials, and so on. Due to the shortcomings of traditional synthesis methods, the design of new materials involving azo molecules at the molecular level requires significant improvements in synthesis methods. This paper reviews the recent research advances in the synthesis of aromatic azo compounds, including symmetric, asymmetric, and cyclic azo compounds, and with an emphasis on the pioneering contribution of functional nanomaterials to the field. We hope that this review will point out the advantages and limitations in the current applications of functional nanomaterials for the synthesis of aromatic azo compounds, and provide new ideas for the preparation of azo compounds and their derivatives. Although the catalysis of nanomaterials can overcome some of the shortcomings of traditional methods, their preparation and cost may limit their large-scale application. Therefore, finding cheaper nanomaterials and improving their recyclability will continue to be an important research direction.

Author Contributions

M.-Y.Z.: Writing—original draft preparation; Y.-F.T.: writing—review and editing; G.-Z.H.: supervision. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

EntryAbbreviationFull name of compound
1HOAcAcetic acid
2DCMDichloromethane
3m-CPBAm-Chloroperbenzoic acid
4DMAP4-Dimethylaminopyridine
5TCCATrichloroisocyanic acid
6NPsNanoparticles
7OC1RDiscrete nanoscopic organic cage
8UVUltraviolet
9NCsNanocrystalline
10h-BNhexagonal Boron nitride
11IPAi-Propyl alcohol
12Ni/GNi/graphene nanocomposite
13NMC-FeFe and N co-doped mesoporous carbon
14MC-FeFe-doped carbon materials
15NMCN-doped carbon materials
16Co-NxCobalt/Nitrogen-doped carbon
17Ni3Fe-MOF-OHSurface hydroxylated Ni3Fe metal-organic frameworks
18TEMPO2,2,6,6-tetramethylpiperidinyl-1-oxide
19NiCo@N-CNTsN-doped carbon nanotube-supported Ni-Co alloy nanoparticles
20N-CNTsN-doped carbon nanotubes
21CQDsCarbon Quantum Dots
22TEOATrolamine
23oxonePotassium peroxomonosulfate
24PHAPhthalhydrazide
25THFTetrahydrofuran
26TBHPt-Butyl hydroperoxide
27EtOHEthanol
28ABTS2,2′-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt

References

  1. Hu, D.; Wang, Y.; Liu, J.; Mao, Y.; Chang, X.; Zhu, Y. Light-Driven Sequential Shape Transformation of Block Copolymer Particles through Three-Dimensional Confined Self-Assembly. Nanoscale 2022, 14, 6291–6298. [Google Scholar] [CrossRef] [PubMed]
  2. Shimizu, T.; Tanifuji, N.; Yoshikawa, H. Azo Compounds as Active Materials of Energy Storage Systems. Angew. Chem. Int. Ed. 2022, 61, e202206093. [Google Scholar] [CrossRef] [PubMed]
  3. Liu, Y.; Zhang, S.; Wu, Y.; Li, W.; Yang, Y. A 3D Adenine-based Cd-MOF: Synthesis, Structure and Photoluminescent Sensing for an Aromatic Azo Compound. Z. Anorg. Allg. Chem. 2020, 646, 1911–1915. [Google Scholar] [CrossRef]
  4. Wibowo, M.; Ding, L. Chemistry and Biology of Natural Azoxy Compounds. J. Nat. Prod. 2020, 83, 3482–3491. [Google Scholar] [CrossRef] [PubMed]
  5. Dembitsky, V.M.; Gloriozova, T.A.; Poroikov, V.V. Pharmacological and Predicted Activities of Natural Azo Compounds. Nat. Prod. Bioprospect. 2017, 7, 151–169. [Google Scholar] [CrossRef]
  6. Zhang, C.; Pi, J.; Chen, S.; Liu, P.; Sun, P. Construction of a 4H-Pyrido [4,3,2-Gh]Phenanthridin-5(6H)-One Skeleton via a Catalyst-Free Radical Cascade Addition/Cyclization Using Azo Compounds as Radical Sources. Org. Chem. Front. 2018, 5, 793–796. [Google Scholar] [CrossRef]
  7. López-Alarcón, C.; Fuentes-Lemus, E.; Figueroa, J.D.; Dorta, E.; Schöneich, C.; Davies, M.J. Azocompounds as Generators of Defined Radical Species: Contributions and Challenges for Free Radical Research. Free. Radic. Biol. Med. 2020, 160, 78–91. [Google Scholar] [CrossRef]
  8. Udoikono, A.D.; Louis, H.; Eno, E.A.; Agwamba, E.C.; Unimuke, T.O.; Igbalagh, A.T.; Edet, H.O.; Odey, J.O.; Adeyinka, A.S. Reactive Azo Compounds as a Potential Chemotherapy Drugs in the Treatment of Malignant Glioblastoma (GBM): Experimental and Theoretical Studies. J. Photochem. Photobiol. 2022, 10, 100116. [Google Scholar] [CrossRef]
  9. Na Joo, H.; Huy Le, B.; Jun Seo, Y. Azo-Pyrene–Based Fluorescent Sensor of Reductive Cleavage of Isomeric Azo Functional Group. Tetrahedron Lett. 2017, 58, 679–681. [Google Scholar] [CrossRef]
  10. Kohei, M.; Takizawa, N.; Tsutsumi, R.; Xu, W.; Kumagai, N. Azo-Tagged C4N4 Fluorophores: Unusual Overcrowded Structures and Their Application to Fluorescent Imaging. Org. Biomol. Chem. 2023, 21, 2889–2893. [Google Scholar] [CrossRef]
  11. Concilio, S.; Iannelli, P.; Sessa, L.; Olivieri, R.; Porta, A.; De Santis, F.; Pantani, R.; Piotto, S. Biodegradable Antimicrobial Films Based on Poly(Lactic Acid) Matrices and Active Azo Compounds. J. Appl. Polym. Sci. 2015, 132, 42357. [Google Scholar] [CrossRef]
  12. Luo, C.; Xu, G.-L.; Ji, X.; Hou, S.; Chen, L.; Wang, F.; Jiang, J.; Chen, Z.; Ren, Y.; Amine, K.; et al. Reversible Redox Chemistry of Azo Compounds for Sodium-Ion Batteries. Angew. Chem. Int. Ed. 2018, 57, 2879–2883. [Google Scholar] [CrossRef]
  13. Li, J.; Huo, F.; Chen, T.; Yan, H.; Yang, Y.; Zhang, S.; Chen, S. In-Situ Construction of Stable Cathode/Li Interfaces Simultaneously via Different Electron Density Azo Compounds for Solid-State Lithium Metal Batteries. Energy Storage Mater. 2021, 40, 394–401. [Google Scholar] [CrossRef]
  14. Adu, J.K.; Amengor, C.D.K.; Mohammed Ibrahim, N.; Amaning-Danquah, C.; Owusu Ansah, C.; Gbadago, D.D.; Sarpong-Agyapong, J. Synthesis and In Vitro Antimicrobial and Anthelminthic Evaluation of Naphtholic and Phenolic Azo Dyes. J. Trop. Med. 2020, 2020, 4850492. [Google Scholar] [CrossRef]
  15. Luo, C.; Borodin, O.; Ji, X.; Hou, S.; Gaskell, K.J.; Fan, X.; Chen, J.; Deng, T.; Wang, R.; Jiang, J.; et al. Azo Compounds as a Family of Organic Electrode Materials for Alkali-Ion Batteries. Proc. Natl. Acad. Sci. USA 2018, 115, 2004–2009. [Google Scholar] [CrossRef] [PubMed]
  16. Fan, F.; Wang, C. Preparation and Photochromic Properties of Nanocapsules Containing Azo Compound with Polyurethane as Wall Material Using in Situ Polymerization. Polym.-Plast. Technol. Eng. 2014, 53, 1062–1069. [Google Scholar] [CrossRef]
  17. Nehls, E.M.; Rosales, A.M.; Anseth, K.S. Enhanced User-Control of Small Molecule Drug Release from a Poly(Ethylene Glycol) Hydrogel via Azobenzene/Cyclodextrin Complex Tethers. J. Mater. Chem. B 2016, 4, 1035–1039. [Google Scholar] [CrossRef]
  18. Xu, G.; Li, S.; Liu, C.; Wu, S. Photoswitchable Adhesives Using Azobenzene-Containing Materials. Chem. Asian J. 2020, 15, 547–554. [Google Scholar] [CrossRef] [PubMed]
  19. Sun, J.; Wang, F.; Zhang, H.; Liu, K. Azobenzene-Based Photomechanical Biomaterials. Adv. NanoBio Res. 2021, 1, 2100020. [Google Scholar] [CrossRef]
  20. Luo, C.; Ji, X.; Chen, J.; Gaskell, K.J.; He, X.; Liang, Y.; Jiang, J.; Wang, C. Solid-State Electrolyte Anchored with a Carboxylated Azo Compound for All-Solid-State Lithium Batteries. Angew. Chem. Int. Ed. 2018, 57, 8567–8571. [Google Scholar] [CrossRef] [PubMed]
  21. Smaniotto, A.; Mezalira, D.Z.; Zapp, E.; Gallardo, H.; Vieira, I.C. Electrochemical Immunosensor Based on an Azo Compound for Thyroid-Stimulating Hormone Detection. Microchem. J. 2017, 133, 510–517. [Google Scholar] [CrossRef]
  22. Peiris, S.; Sarina, S.; Han, C.; Xiao, Q.; Zhu, H.-Y. Silver and Palladium Alloy Nanoparticle Catalysts: Reductive Coupling of Nitrobenzene through Light Irradiation. Dalton Trans. 2017, 46, 10665–10672. [Google Scholar] [CrossRef] [PubMed]
  23. Chong, X.; Liu, C.; Huang, Y.; Huang, C.; Zhang, B. Potential-Tuned Selective Electrosynthesis of Azoxy-, Azo- and Amino-Aromatics over a CoP Nanosheet Cathode. Natl. Sci. Rev. 2020, 7, 285–295. [Google Scholar] [CrossRef] [PubMed]
  24. Chaiseeda, K.; Nishimura, S.; Ebitani, K. Gold Nanoparticles Supported on Alumina as a Catalyst for Surface Plasmon-Enhanced Selective Reductions of Nitrobenzene. ACS Omega 2017, 2, 7066–7070. [Google Scholar] [CrossRef] [PubMed]
  25. Yadav, G.D.; Mewada, R.K. Novelties of Azobenzene Synthesis via Selective Hydrogenation of Nitrobenzene over Nano-Fibrous Ag-OMS-2—Mechanism and Kinetics. Chem. Eng. J. 2013, 221, 500–511. [Google Scholar] [CrossRef]
  26. Arora, A.; Oswal, P.; Kumar Rao, G.; Kumar, S.; Kumar, A. Organoselenium Ligands for Heterogeneous and Nanocatalytic Systems: Development and Applications. Dalton Trans. 2021, 50, 8628–8656. [Google Scholar] [CrossRef]
  27. Pothula, K.; Tang, L.; Zha, Z.; Wang, Z. Bismuth Nanoparticles: An Efficient Catalyst for Reductive Coupling of Nitroarenes to Azo-Compounds. RSC Adv. 2015, 5, 83144–83148. [Google Scholar] [CrossRef]
  28. Agnoli, S. Interfacial Chemistry of Low-Dimensional Systems for Applications in Nanocatalysis. Eur. J. Inorg. Chem. 2018, 2018, 4311–4321. [Google Scholar] [CrossRef]
  29. Zou, Y.; Zhang, M.; Cao, F.; Li, J.; Zhang, S.; Qu, Y. Single Crystal MnOOH Nanotubes for Selective Oxidative Coupling of Anilines to Aromatic Azo Compounds. J. Mater. Chem. A 2021, 9, 19692–19697. [Google Scholar] [CrossRef]
  30. Liu, X.; Ye, S.; Li, H.-Q.; Liu, Y.-M.; Cao, Y.; Fan, K.-N. Mild, selective and switchable transfer reduction of nitroarenes catalyzed by supported gold nanoparticles. Catal. Sci. Technol. 2013, 3, 3200. [Google Scholar] [CrossRef]
  31. Teng, Y.; Wang, X.; Wang, M.; Liu, Q.; Shao, Y.; Li, H.; Liang, C.; Chen, X.; Wang, H. A Schiff-Base Modified Pt Nano-Catalyst for Highly Efficient Synthesis of Aromatic Azo Compounds. Catalysts 2019, 9, 339. [Google Scholar] [CrossRef]
  32. Gao, S.; Han, Y.; Fan, M.; Li, Z.; Ge, K.; Liang, X.-J.; Zhang, J. Metal-Organic Framework-Based Nanocatalytic Medicine for Chemodynamic Therapy. Sci. China Mater. 2020, 63, 2429–2434. [Google Scholar] [CrossRef]
  33. Ingale, G.; Seo, Y.J. Azo Compounds with Different Sized Fluorophores and Characterization of Their Photophysical Properties Based on Trans to Cis Conformational Change. Tetrahedron Lett. 2014, 55, 5247–5250. [Google Scholar] [CrossRef]
  34. Grebenkin, S.Y.; Syutkin, V.M.; Baranov, D.S. Mutual Orientation of the n → π * and π → π * Transition Dipole Moments in Azo Compounds: Determination by Light-Induced Optical Anisotropy. J. Photochem. Photobiol. A Chem. 2017, 344, 1–7. [Google Scholar] [CrossRef]
  35. Rezaei-Seresht, E.; Mireskandari, E.; Kheirabadi, M.; Cheshomi, H.; Rezaei-Seresht, H.; Aldaghi, L.S. Synthesis and Anticancer Activity of New Azo Compounds Containing Extended π-Conjugated Systems. Chem. Pap. 2017, 71, 1463–1469. [Google Scholar] [CrossRef]
  36. Bandara, H.M.D.; Burdette, S.C. Photoisomerization in Different Classes of Azobenzene. Chem. Soc. Rev. 2012, 41, 1809–1825. [Google Scholar] [CrossRef]
  37. Sarkar, S.; Sarkar, P.; Ghosh, P. Selective Single-Step Oxidation of Amine to Cross-Azo Compounds with an Unhampered Primary Benzyl Alcohol Functionality. Org. Lett. 2018, 20, 6725–6729. [Google Scholar] [CrossRef]
  38. Yang, Y.; Li, S.; Xie, C.; Liu, H.; Wang, Y.; Mei, Q.; Liu, H.; Han, B. Ethylenediamine Promoted the Hydrogenative Coupling of Nitroarenes over Ni/C Catalyst. Chin. Chem. Lett. 2019, 30, 203–206. [Google Scholar] [CrossRef]
  39. Dana, S.; Sahoo, H.; Bhattacharyya, A.; Mandal, A.; Prasad, E.; Baidya, M. Copper-Catalyzed Chelation-Assisted Synthesis of Unsymmetrical Aliphatic Azo Compounds. ChemistrySelect 2017, 2, 2029–2033. [Google Scholar] [CrossRef]
  40. Zhou, X.; Yang, Y.; Wang, J.; Ren, W.; Liu, S.; Zheng, C.; Gao, X. Enhancing Nitrobenzene Reduction to Azoxybenzene by Regulating the O-Vacancy Defects over Rationally Tailored CeO2 Nanocrystals. Appl. Surf. Sci. 2022, 572, 151343. [Google Scholar] [CrossRef]
  41. Zhang, Y.; Huang, C.; Lin, X.; Hu, Q.; Hu, B.; Zhou, Y.; Zhu, G. Modular Synthesis of Alkylarylazo Compounds via Iron(III)-Catalyzed Olefin Hydroamination. Org. Lett. 2019, 21, 2261–2264. [Google Scholar] [CrossRef] [PubMed]
  42. Liu, Y.; Liu, B.; Guo, A.; Dong, Z.; Jin, S.; Lu, Y. Reduction of Nitroarenes to Azoxybenzenes by Potassium Borohydride in Water. Molecules 2011, 16, 3563–3568. [Google Scholar] [CrossRef] [PubMed]
  43. Da Silva, M.A.R.; Rocha, G.F.S.R.; Diab, G.A.A.; Cunha, C.S.; Pastana, V.G.S.; Teixeira, I.F. Simple and Straightforward Method to Prepare Highly Dispersed Ni Sites for Selective Nitrobenzene Coupling to Azo/Azoxy Compounds. Chem. Eng. J. 2023, 460, 141068. [Google Scholar] [CrossRef]
  44. Han, S.; Cheng, Y.; Liu, S.; Tao, C.; Wang, A.; Wei, W.; Yu, H.; Wei, Y. Selective Oxidation of Anilines to Azobenzenes and Azoxybenzenes by a Molecular Mo Oxide Catalyst. Angew. Chem. Int. Ed. 2021, 60, 6382–6385. [Google Scholar] [CrossRef] [PubMed]
  45. Doherty, S.; Knight, J.G.; Backhouse, T.; Summers, R.J.; Abood, E.; Simpson, W.; Paget, W.; Bourne, R.A.; Chamberlain, T.W.; Stones, R.; et al. Highly Selective and Solvent-Dependent Reduction of Nitrobenzene to N-Phenylhydroxylamine, Azoxybenzene, and Aniline Catalyzed by Phosphino-Modified Polymer Immobilized Ionic Liquid-Stabilized AuNPs. ACS Catal. 2019, 9, 4777–4791. [Google Scholar] [CrossRef]
  46. Chen, W.; Li, H.; Jin, Y.; Wu, C.; Yuan, Z.; Ma, P.; Wang, J.; Niu, J. An Intriguing Tetranuclear Rh-Based Polyoxometalate for the Reduction of Nitroarene and Oxidation of Aniline. Chem. Commun. 2022, 58, 9902–9905. [Google Scholar] [CrossRef] [PubMed]
  47. Liu, X.; Li, H.-Q.; Ye, S.; Liu, Y.-M.; He, H.-Y.; Cao, Y. Gold-Catalyzed Direct Hydrogenative Coupling of Nitroarenes to Synthesize Aromatic Azo Compounds. Angew. Chem. Int. Ed. 2014, 53, 7624–7628. [Google Scholar] [CrossRef]
  48. Shen, J.; Xu, J.; Zhu, Q.; Zhang, P. Hypervalent Iodine(iii)-Promoted Rapid Cascade Reaction for the Synthesis of Unsymmetric Azo Compounds. Org. Biomol. Chem. 2021, 19, 3119–3123. [Google Scholar] [CrossRef]
  49. Shen, J.; Xu, J.; He, L.; Ouyang, Y.; Huang, L.; Li, W.; Zhu, Q.; Zhang, P. Photoinduced Rapid Multicomponent Cascade Reaction of Aryldiazonium Salts with Unactivated Alkenes and TMSN3. Org. Lett. 2021, 23, 1204–1208. [Google Scholar] [CrossRef]
  50. Khaligh, N.G.; Hamid, S.B.A.; Johari, S. Telescopic Synthesis of Azo Compounds via Stable Arenediazonium Tosylates by Using n-Butyl Nitrite as Diazotization Reagent. Polycycl. Aromat. Compd. 2019, 39, 346–352. [Google Scholar] [CrossRef]
  51. Wang, Y.; Yihuo, A.; Wang, L.; Dong, S.; Feng, X. Catalytic Asymmetric Synthesis of Chiral Azo Compounds via Interrupted Japp-Klingemann Reaction with Aryldiazonium Salts. Sci. China Chem. 2022, 65, 546–553. [Google Scholar] [CrossRef]
  52. Hu, J.; Song, T.; Yu, M.-M.; Yu, H. Optically Controlled Solid-to-Liquid Phase Transition Materials Based on Azo Compounds. Chem. Mater. 2023, 35, 4621–4648. [Google Scholar] [CrossRef]
  53. An, Y.; Tan, H.; Zhao, S. Ag2 CO3 Mediated Oxidative Dehydrogenative Coupling of Anilines Giving Aromatic Azo Compounds. Chin. J. Org. Chem. 2017, 37, 226. [Google Scholar] [CrossRef]
  54. Monir, K.; Ghosh, M.; Mishra, S.; Majee, A.; Hajra, A. Phenyliodine(III) Diacetate (PIDA) Mediated Synthesis of Aromatic Azo Compounds through Oxidative Dehydrogenative Coupling of Anilines: Scope and Mechanism: PIDA-Mediated Synthesis of Aromatic Azo Compounds. Eur. J. Org. Chem. 2014, 2014, 1096–1102. [Google Scholar] [CrossRef]
  55. Antoine John, A.; Lin, Q. Synthesis of Azobenzenes Using N-Chlorosuccinimide and 1,8-Diazabicyclo[5.4.0]Undec-7-Ene (DBU). J. Org. Chem. 2017, 82, 9873–9876. [Google Scholar] [CrossRef]
  56. Sarkar, P.; Mukhopadhyay, C. First Use of P-Tert-Butylcalix[4]Arene-Tetra-O-Acetate as a Nanoreactor Having Tunable Selectivity towards Cross Azo-Compounds by Trapping Silver Ions. Green. Chem. 2016, 18, 442–451. [Google Scholar] [CrossRef]
  57. Amtawong, J.; Balcells, D.; Wilcoxen, J.; Handford, R.C.; Biggins, N.; Nguyen, A.I.; Britt, R.D.; Tilley, T.D. Isolation and Study of Ruthenium–Cobalt Oxo Cubanes Bearing a High-Valent, Terminal RuV–Oxo with Significant Oxyl Radical Character. J. Am. Chem. Soc. 2019, 141, 19859–19869. [Google Scholar] [CrossRef]
  58. Qin, H.; Liu, C.; Lv, N.; He, W.; Meng, J.; Fang, Z.; Guo, K. Continuous and Green Microflow Synthesis of Azobenzene Compounds Catalyzed by Consecutively Prepared Tetrahedron CuBr. Dye. Pigment. 2020, 174, 108071. [Google Scholar] [CrossRef]
  59. Hu, L.; Cao, X.; Chen, L.; Zheng, J.; Lu, J.; Sun, X.; Gu, H. Highly Efficient Synthesis of Aromatic Azos Catalyzed by Unsupported Ultra-Thin Pt Nanowires. Chem. Commun. 2012, 48, 3445. [Google Scholar] [CrossRef]
  60. Ötvös, S.B.; Georgiádes, Á.; Mészáros, R.; Kis, K.; Pálinkó, I.; Fülöp, F. Continuous-Flow Oxidative Homocouplings without Auxiliary Substances: Exploiting a Solid Base Catalyst. J. Catal. 2017, 348, 90–99. [Google Scholar] [CrossRef]
  61. Oseghale, C.O.; Fapojuwo, D.P.; Alimi, O.A.; Akinnawo, C.A.; Mogudi, B.M.; Onisuru, O.R.; Meijboom, R. Bifunctional Cs−Au/Co3O4 (Basic and Redox)-Catalyzed Oxidative Synthesis of Aromatic Azo Compounds from Anilines. Eur. J. Org. Chem. 2021, 2021, 5063–5073. [Google Scholar] [CrossRef]
  62. Wang, J.; He, J.; Zhi, C.; Luo, B.; Li, X.; Pan, Y.; Cao, X.; Gu, H. Highly Efficient Synthesis of Azos Catalyzed by the Common Metal Copper (0) through Oxidative Coupling Reactions. RSC Adv. 2014, 4, 16607. [Google Scholar] [CrossRef]
  63. Zhang, X.; Yao, J.; Ke, X. Tuning Catalytic Selectivity in Cascade Reactions by Light Irradiation. Catal. Lett. 2018, 148, 1124–1129. [Google Scholar] [CrossRef]
  64. Saha, A.; Payra, S.; Selvaratnam, B.; Bhattacharya, S.; Pal, S.; Koodali, R.T.; Banerjee, S. Hierarchical Mesoporous RuO2/Cu2O Nanoparticle-Catalyzed Oxidative Homo/Hetero Azo-Coupling of Anilines. ACS Sustain. Chem. Eng. 2018, 6, 11345–11352. [Google Scholar] [CrossRef]
  65. Cai, S.; Rong, H.; Yu, X.; Liu, X.; Wang, D.; He, W.; Li, Y. Room Temperature Activation of Oxygen by Monodispersed Metal Nanoparticles: Oxidative Dehydrogenative Coupling of Anilines for Azobenzene Syntheses. ACS Catal. 2013, 3, 478–486. [Google Scholar] [CrossRef]
  66. Yaghoubian, A.; Hodgson, G.K.; Adler, M.J.; Impellizzeri, S. Direct Photochemical Route to Azoxybenzenes via Nitroarene Homocoupling. Org. Biomol. Chem. 2022, 20, 7332–7337. [Google Scholar] [CrossRef] [PubMed]
  67. Ma, Y.; Wu, S.; Jiang, S.; Xiao, F.; Deng, G. Electrosynthesis of Azobenzenes Directly from Nitrobenzenes. Chin. J. Chem. 2021, 39, 3334–3338. [Google Scholar] [CrossRef]
  68. Ke, X.; Zhang, X.; Zhao, J.; Sarina, S.; Barry, J.; Zhu, H. Selective Reductions Using Visible Light Photocatalysts of Supported Gold Nanoparticles. Green. Chem. 2013, 15, 236–244. [Google Scholar] [CrossRef]
  69. Tran, V.H.; Kim, H.-K. Visible-Light-Driven SAQS-Catalyzed Aerobic Oxidative Dehydrogenation of Alkyl 2-Phenylhydrazinecarboxylates. RSC Adv. 2022, 12, 30304–30309. [Google Scholar] [CrossRef]
  70. Du, K.-S.; Huang, J.-M. Electrochemical Dehydrogenation of Hydrazines to Azo Compounds. Green. Chem. 2019, 21, 1680–1685. [Google Scholar] [CrossRef]
  71. Luo, C.; Ji, X.; Hou, S.; Eidson, N.; Fan, X.; Liang, Y.; Deng, T.; Jiang, J.; Wang, C. Azo Compounds Derived from Electrochemical Reduction of Nitro Compounds for High Performance Li-Ion Batteries. Adv. Mater. 2018, 30, 1706498. [Google Scholar] [CrossRef]
  72. He, Y.; Shangguan, Z.; Zhang, Z.; Xie, M.; Yu, C.; Li, T. Azobispyrazole Family as Photoswitches Combining (Near-) Quantitative Bidirectional Isomerization and Widely Tunable Thermal Half-Lives from Hours to Years**. Angew. Chem. Int. Ed. 2021, 60, 16539–16546. [Google Scholar] [CrossRef] [PubMed]
  73. Yoshida, Y.; Ida, H.; Mino, T.; Sakamoto, M. Formal [3 + 2] Cycloaddition of α-Imino Esters with Azo Compounds: Facile Construction of Pentasubstituted 1,2,4-Triazoline Skeletons. Molecules 2023, 28, 4339. [Google Scholar] [CrossRef] [PubMed]
  74. Ye, D.; Liu, L.; Peng, Q.; Qiu, J.; Gong, H.; Zhong, A.; Liu, S. Effect of Controlling Thiophene Rings on D-A Polymer Photocatalysts Accessed via Direct Arylation for Hydrogen Production. Molecules 2023, 28, 4507. [Google Scholar] [CrossRef] [PubMed]
  75. Dutta, B.; Biswas, S.; Sharma, V.; Savage, N.O.; Alpay, S.P.; Suib, S.L. Mesoporous Manganese Oxide Catalyzed Aerobic Oxidative Coupling of Anilines to Aromatic Azo Compounds. Angew. Chem. Int. Ed. 2016, 55, 2171–2175. [Google Scholar] [CrossRef] [PubMed]
  76. Jiang, B.; Du, Y.-Y.; Han, G.-Z. Palladium-Mediated Base-Free and Solvent-Free Synthesis of Aromatic Azo Compounds from Anilines Catalyzed by Copper Acetate. Green. Process. Synth. 2022, 11, 823–829. [Google Scholar] [CrossRef]
  77. Maier, M.S.; Hüll, K.; Reynders, M.; Matsuura, B.S.; Leippe, P.; Ko, T.; Schäffer, L.; Trauner, D. Oxidative Approach Enables Efficient Access to Cyclic Azobenzenes. J. Am. Chem. Soc. 2019, 141, 17295–17304. [Google Scholar] [CrossRef]
  78. Shukla, A.; Singha, R.K.; Konathala, L.N.S.; Sasaki, T.; Bal, R. Catalytic Oxidation of Aromatic Amines to Azoxy Compounds over a Cu–CeO 2 Catalyst Using H2O2 as an Oxidant. RSC Adv. 2016, 6, 22812–22820. [Google Scholar] [CrossRef]
  79. Kim, M.H.; Kim, J. Aerobic Oxidation of Alkyl 2-Phenylhydrazinecarboxylates Catalyzed by CuCl and DMAP. J. Org. Chem. 2018, 83, 1673–1679. [Google Scholar] [CrossRef]
  80. Su, Y.; Liu, X.; Yu, J.; Cao, G.; Zhang, R.; Zhao, Y.; Huang, D.; Wang, K.-H.; Huo, C.; Hu, Y. Trichloroisocyanuric Acid Mediated Oxidative Dehydrogenation of Hydrazines: A Practical Chemical Oxidation to Access Azo Compounds. Synthesis 2020, 52, 1103–1112. [Google Scholar] [CrossRef]
  81. Jiang, B.; Ning, Y.; Fan, W.; Tu, S.-J.; Li, G. Oxidative Dehydrogenative Couplings of Pyrazol-5-Amines Selectively Forming Azopyrroles. J. Org. Chem. 2014, 79, 4018–4024. [Google Scholar] [CrossRef] [PubMed]
  82. Mondal, B.; Mukherjee, P.S. Cage Encapsulated Gold Nanoparticles as Heterogeneous Photocatalyst for Facile and Selective Reduction of Nitroarenes to Azo Compounds. J. Am. Chem. Soc. 2018, 140, 12592–12601. [Google Scholar] [CrossRef] [PubMed]
  83. Yan, Z.; Xie, X.; Song, Q.; Ma, F.; Sui, X.; Huo, Z.; Ma, M. Tandem Selective Reduction of Nitroarenes Catalyzed by Palladium Nanoclusters. Green. Chem. 2020, 22, 1301–1307. [Google Scholar] [CrossRef]
  84. Liu, Q.; Xu, Y.; Qiu, X.; Huang, C.; Liu, M. Chemoselective Hydrogenation of Nitrobenzenes Activated with Tuned Au/h-BN. J. Catal. 2019, 370, 55–60. [Google Scholar] [CrossRef]
  85. Pahalagedara, M.N.; Pahalagedara, L.R.; He, J.; Miao, R.; Gottlieb, B.; Rathnayake, D.; Suib, S.L. Room Temperature Selective Reduction of Nitrobenzene to Azoxybenzene over Magnetically Separable Urchin-like Ni/Graphene Nanocomposites. J. Catal. 2016, 336, 41–48. [Google Scholar] [CrossRef]
  86. Wang, J.; Yu, X.; Shi, C.; Lin, D.; Li, J.; Jin, H.; Chen, X.; Wang, S. Iron and Nitrogen Co-Doped Mesoporous Carbon-Based Heterogeneous Catalysts for Selective Reduction of Nitroarenes. Adv. Synth. Catal. 2019, 361, 3525–3531. [Google Scholar] [CrossRef]
  87. Moran, M.J.; Martina, K.; Baricco, F.; Tagliapietra, S.; Manzoli, M.; Cravotto, G. Tuneable Copper Catalysed Transfer Hydrogenation of Nitrobenzenes to Aniline or Azo Derivatives. Adv. Synth. Catal. 2020, 362, 2689–2700. [Google Scholar] [CrossRef]
  88. Hu, L.; Cao, X.; Shi, L.; Qi, F.; Guo, Z.; Lu, J.; Gu, H. A Highly Active Nano-Palladium Catalyst for the Preparation of Aromatic Azos under Mild Conditions. Org. Lett. 2011, 13, 5640–5643. [Google Scholar] [CrossRef]
  89. Huang, R.; Wang, Y.; Liu, X.; Zhou, P.; Jin, S.; Zhang, Z. Co–N x Catalyst: An Effective Catalyst for the Transformation of Nitro Compounds into Azo Compounds. React. Chem. Eng. 2021, 6, 112–118. [Google Scholar] [CrossRef]
  90. Qiao, W.; Waseem, I.; Shang, G.; Wang, D.; Li, Y.; Besenbacher, F.; Niemantsverdriet, H.; Yan, C.; Su, R. Paired Electrochemical N–N Coupling Employing a Surface-Hydroxylated Ni3 Fe-MOF-OH Bifunctional Electrocatalyst with Enhanced Adsorption of Nitroarenes and Anilines. ACS Catal. 2021, 11, 13510–13518. [Google Scholar] [CrossRef]
  91. Gong, W.; Mao, X.; Zhang, J.; Lin, Y.; Zhang, H.; Du, A.; Xiong, Y.; Zhao, H. Ni–Co Alloy Nanoparticles Catalyze Selective Electrochemical Coupling of Nitroarenes into Azoxybenzene Compounds in Aqueous Electrolyte. ACS Nano 2023, 17, 3984–3995. [Google Scholar] [CrossRef] [PubMed]
  92. Zhang, Y.-F.; Mellah, M. Convenient Electrocatalytic Synthesis of Azobenzenes from Nitroaromatic Derivatives Using SmI2. ACS Catal. 2017, 7, 8480–8486. [Google Scholar] [CrossRef]
  93. Zhou, B.; Song, J.; Wu, T.; Liu, H.; Xie, C.; Yang, G.; Han, B. Simultaneous and Selective Transformation of Glucose to Arabinose and Nitrosobenzene to Azoxybenzene Driven by Visible-Light. Green. Chem. 2016, 18, 3852–3857. [Google Scholar] [CrossRef]
  94. Wang, B.; Deng, Z.; Li, Z. Efficient Chemoselective Hydrogenation of Nitrobenzene to Aniline, Azoxybenzene and Azobenzene over CQDs/ZnIn2S4 Nanocomposites under Visible Light. J. Catal. 2020, 389, 241–246. [Google Scholar] [CrossRef]
  95. Sousa, A.C.; Baptista, S.R.; Martins, L.O.; Robalo, M.P. Synthesis of Azobenzene Dyes Mediated by CotA Laccase. Chem. Asian J. 2019, 14, 187–193. [Google Scholar] [CrossRef]
  96. Pariyar, G.C.; Kundu, T.; Mitra, B.; Mukherjee, S.; Ghosh, P. Ethyl Lactate: An Efficient Green Mediator for Transition Metal Free Synthesis of Symmetric and Unsymmetric Azobenzenes. ChemistrySelect 2020, 5, 9781–9786. [Google Scholar] [CrossRef]
  97. Xie, R.; Xiao, Y.; Wang, Y.; Xu, Z.-W.; Tian, N.; Li, S.; Zeng, M.-H. Hydrazine–Halogen Exchange Strategy Toward N=N-Containing Compounds and Process Tracking for Mechanistic Insight. Org. Lett. 2023, 25, 2415–2419. [Google Scholar] [CrossRef]
  98. Finck, L.; Oestreich, M. Synthesis of Non-Symmetric Azoarenes by Palladium-Catalyzed Cross-Coupling of Silicon-Masked Diazenyl Anions and (Hetero)Aryl Halides. Angew. Chem. Int. Ed. 2022, 61, e202210907. [Google Scholar] [CrossRef]
Molecules 28 06741 sch001
Scheme 1. Traditional synthetic method of aromatic azo compounds.
Scheme 1. Traditional synthetic method of aromatic azo compounds.
Molecules 28 06741 sch001
Molecules 28 06741 g001
Figure 1. Trend of the number of articles on aromatic azo compounds in the last ten years (these data were obtained from Web of Science).
Figure 1. Trend of the number of articles on aromatic azo compounds in the last ten years (these data were obtained from Web of Science).
Molecules 28 06741 g001
Molecules 28 06741 g002
Figure 2. Synthetic mechanism of aromatic azo compounds from aniline catalyzed by mesoporous manganese oxide materials [75]. (The optimal reaction conditions: aniline (1 mmol); meso-Mn2O3 (0.32 mmol); toluene as the solvent; 110 °C; air balloon).
Figure 2. Synthetic mechanism of aromatic azo compounds from aniline catalyzed by mesoporous manganese oxide materials [75]. (The optimal reaction conditions: aniline (1 mmol); meso-Mn2O3 (0.32 mmol); toluene as the solvent; 110 °C; air balloon).
Molecules 28 06741 g002
Molecules 28 06741 g003
Figure 3. Our previous work on oxidation coupling of aniline to form azo compounds [76]. (The optimal reaction conditions: aniline (1 mmol); Cu (OAc)2 (10 mol %); PdCl2 (1 mol %); 100 °C; 8 h; air).
Figure 3. Our previous work on oxidation coupling of aniline to form azo compounds [76]. (The optimal reaction conditions: aniline (1 mmol); Cu (OAc)2 (10 mol %); PdCl2 (1 mol %); 100 °C; 8 h; air).
Molecules 28 06741 g003
Molecules 28 06741 g004
Figure 4. Schematic diagram of the synthesis of cyclic aromatic azo compounds [77]. (The optimal reaction conditions: 2,2′-ethylenedianiline (1.178 mmol); m-CPBA (2 mmol); AcOH/DCM (1:1); room temperature).
Figure 4. Schematic diagram of the synthesis of cyclic aromatic azo compounds [77]. (The optimal reaction conditions: 2,2′-ethylenedianiline (1.178 mmol); m-CPBA (2 mmol); AcOH/DCM (1:1); room temperature).
Molecules 28 06741 g004
Molecules 28 06741 g005
Figure 5. Highly selective synthesis of azoxybenzene via oxidation of aniline catalyzed by 3.8% Cu-CeO2 [78]. (The optimal reaction conditions: aniline (1 g); acetonitrile (15 mL); aniline/H2O2 (1:3); 3.8% Cu-CeO2 (0.1g); 50 °C; 6 h).
Figure 5. Highly selective synthesis of azoxybenzene via oxidation of aniline catalyzed by 3.8% Cu-CeO2 [78]. (The optimal reaction conditions: aniline (1 g); acetonitrile (15 mL); aniline/H2O2 (1:3); 3.8% Cu-CeO2 (0.1g); 50 °C; 6 h).
Molecules 28 06741 g005
Molecules 28 06741 g006
Figure 6. Cu-Catalyzed aerobic oxidation of ethyl 2-Phenylhydrazinecarboxylate [79]. (The optimal reaction conditions: ethyl 2-phenylhydrazinecarboxylate (0.5 mmol); CuCl (5 mol %); DMAP (10 mmol %); CH2Cl2 (2 mL); air; room temperature; 3 h).
Figure 6. Cu-Catalyzed aerobic oxidation of ethyl 2-Phenylhydrazinecarboxylate [79]. (The optimal reaction conditions: ethyl 2-phenylhydrazinecarboxylate (0.5 mmol); CuCl (5 mol %); DMAP (10 mmol %); CH2Cl2 (2 mL); air; room temperature; 3 h).
Molecules 28 06741 g006
Molecules 28 06741 g007
Figure 7. Oxidation of aromatic hydrazine by TCCA to form azo compounds [80]. (The optimal reaction conditions: diphenylhydrazine (0.3 mmol); TCCA (0.6 mmol); THF (1.5 mL); air; room temperature; 15 min).
Figure 7. Oxidation of aromatic hydrazine by TCCA to form azo compounds [80]. (The optimal reaction conditions: diphenylhydrazine (0.3 mmol); TCCA (0.6 mmol); THF (1.5 mL); air; room temperature; 15 min).
Molecules 28 06741 g007
Molecules 28 06741 g008
Figure 8. Oxidative dehydrogenative coupling strategy of pyrazol-5-amines for the selective formation of functionalized heteroaromatic azo compounds [81]. (The optimal reaction conditions of azopyrrole derivatives: pyrazol-5-amines (1 mmol); TBHP (4 mmol); I2 (1.1 mmol); EtOH, K2CO3 (1.5 mmol); air, 50 °C. The optimal reaction conditions of azopyrroles: pyrazol-5-amines (1 mmol); TBHP (3 mmol); 1,10-phenanthroline (30 mol%); CH2Cl2, CuI (10 mol %); air; room temperature).
Figure 8. Oxidative dehydrogenative coupling strategy of pyrazol-5-amines for the selective formation of functionalized heteroaromatic azo compounds [81]. (The optimal reaction conditions of azopyrrole derivatives: pyrazol-5-amines (1 mmol); TBHP (4 mmol); I2 (1.1 mmol); EtOH, K2CO3 (1.5 mmol); air, 50 °C. The optimal reaction conditions of azopyrroles: pyrazol-5-amines (1 mmol); TBHP (3 mmol); 1,10-phenanthroline (30 mol%); CH2Cl2, CuI (10 mol %); air; room temperature).
Molecules 28 06741 g008
Molecules 28 06741 g009
Figure 9. Synthesis of aromatic azo compounds by photocatalytic reduction of nitroaromatics [82]. The optimal reaction conditions: nitroarenes (1 mmol); NaOH (0.2 mmol); Au@OC1R (0.5 mol % Au); 2-propanol (15 mL); N2; 120 min; 30 °C).
Figure 9. Synthesis of aromatic azo compounds by photocatalytic reduction of nitroaromatics [82]. The optimal reaction conditions: nitroarenes (1 mmol); NaOH (0.2 mmol); Au@OC1R (0.5 mol % Au); 2-propanol (15 mL); N2; 120 min; 30 °C).
Molecules 28 06741 g009
Molecules 28 06741 g010
Figure 10. The tandem reduction strategy for the selective conversion of nitroaromatics [83]. (The optimal reaction conditions: p-nitrotoluene (1 mmol); Pd(OAc)2 (0.1 mol %); NaBH4 (2 mmol); H2O/EtOH (2:3); room temperature; O2).
Figure 10. The tandem reduction strategy for the selective conversion of nitroaromatics [83]. (The optimal reaction conditions: p-nitrotoluene (1 mmol); Pd(OAc)2 (0.1 mol %); NaBH4 (2 mmol); H2O/EtOH (2:3); room temperature; O2).
Molecules 28 06741 g010
Molecules 28 06741 g011
Figure 11. The reduction of nitrobenzene catalyzed by Au/BN [84]. (The optimal reaction conditions: nitrobenzene (0.31 mmol); KOH (0.06 mmol); i-propyl alcohol (3 mL); 20.9% Au-BN (10 mg); 50 °C; 15 min).
Figure 11. The reduction of nitrobenzene catalyzed by Au/BN [84]. (The optimal reaction conditions: nitrobenzene (0.31 mmol); KOH (0.06 mmol); i-propyl alcohol (3 mL); 20.9% Au-BN (10 mg); 50 °C; 15 min).
Molecules 28 06741 g011
Molecules 28 06741 g012
Figure 12. Mechanism of Ni/graphene-catalyzed reduction of nitrobenzene [85]. (The optimal reaction conditions: nitrobenzene (15 mmol); EtOH (5 mL); N2H4·H2O (22.5 mmol); Ni/G (10 mg); room temperature; 2 h).
Figure 12. Mechanism of Ni/graphene-catalyzed reduction of nitrobenzene [85]. (The optimal reaction conditions: nitrobenzene (15 mmol); EtOH (5 mL); N2H4·H2O (22.5 mmol); Ni/G (10 mg); room temperature; 2 h).
Molecules 28 06741 g012
Molecules 28 06741 g013
Figure 13. Reduction of nitroaromatics catalyzed by Fe and N co-doped mesoporous carbon [86]. (The optimal reaction conditions: 1-chloro-4-nitrobenzene (1.0 mmol); N2H4·H2O (1.65 mmol); KOH (1.5 mmol) and NMC-Fe (45 mg); toluene (1 mL); 100 °C; 1 h).
Figure 13. Reduction of nitroaromatics catalyzed by Fe and N co-doped mesoporous carbon [86]. (The optimal reaction conditions: 1-chloro-4-nitrobenzene (1.0 mmol); N2H4·H2O (1.65 mmol); KOH (1.5 mmol) and NMC-Fe (45 mg); toluene (1 mL); 100 °C; 1 h).
Molecules 28 06741 g013
Molecules 28 06741 g014
Figure 14. Controlled reduction of nitrobenzene catalyzed by CuNPs with different hydrogen sources [87]. (The optimal reaction conditions: nitroarene (3 mmol); ethanolamine (20 mL); KOH (6 mmol); CuNPs (5 mol %); 55 °C; 20–24 h).
Figure 14. Controlled reduction of nitrobenzene catalyzed by CuNPs with different hydrogen sources [87]. (The optimal reaction conditions: nitroarene (3 mmol); ethanolamine (20 mL); KOH (6 mmol); CuNPs (5 mol %); 55 °C; 20–24 h).
Molecules 28 06741 g014
Molecules 28 06741 g015
Figure 15. Mechanism of Pd-catalyzed reduction of nitrobenzene [88]. (The optimal reaction conditions: nitroarene (1 mmol); p-xylene (2 mL); KOH (1 mmol); nano-Pd (1 mg); 120 °C; H2; 24 h).
Figure 15. Mechanism of Pd-catalyzed reduction of nitrobenzene [88]. (The optimal reaction conditions: nitroarene (1 mmol); p-xylene (2 mL); KOH (1 mmol); nano-Pd (1 mg); 120 °C; H2; 24 h).
Molecules 28 06741 g015
Molecules 28 06741 g016
Figure 16. Pathways by which nitrobenzene is reduced [89]. (The optimal reaction conditions: nitro compound (1 mmol); Co–Nx/C-800-AT catalyst (40 mg); ethanol (10 mL); H2 (2.5 bar); NaOH (0.5 mmol); 110 °C, 2–4 h).
Figure 16. Pathways by which nitrobenzene is reduced [89]. (The optimal reaction conditions: nitro compound (1 mmol); Co–Nx/C-800-AT catalyst (40 mg); ethanol (10 mL); H2 (2.5 bar); NaOH (0.5 mmol); 110 °C, 2–4 h).
Molecules 28 06741 g016
Molecules 28 06741 g017
Figure 17. Synthesis of azobenzene by electrochemical synthesis using Ni3Fe-MOF-OH as electrodes [90]. (The optimal reaction conditions: nitroaromatics (8 mmol); anilines (12 mmol); KOH (1 mol); TEMPO (8 mmol); Ni3Fe-MOF-OH; 1.4 V; 3 h).
Figure 17. Synthesis of azobenzene by electrochemical synthesis using Ni3Fe-MOF-OH as electrodes [90]. (The optimal reaction conditions: nitroaromatics (8 mmol); anilines (12 mmol); KOH (1 mol); TEMPO (8 mmol); Ni3Fe-MOF-OH; 1.4 V; 3 h).
Molecules 28 06741 g017
Molecules 28 06741 g018
Figure 18. Schematic diagram of NiCo@N-CNTs||Ni(OH)2/NF dual electrode electrolyzer [91]. (The optimal reaction conditions: nitroarenes (25 mmol); KOH (1 mol); NiCo@N-CNTs; 0.8 V; room temperature; 7–11 h).
Figure 18. Schematic diagram of NiCo@N-CNTs||Ni(OH)2/NF dual electrode electrolyzer [91]. (The optimal reaction conditions: nitroarenes (25 mmol); KOH (1 mol); NiCo@N-CNTs; 0.8 V; room temperature; 7–11 h).
Molecules 28 06741 g018
Molecules 28 06741 g019
Figure 19. Electrocatalytic reduction of nitrobenzene using SmI2 as electrode [92]. (The optimal reaction conditions: nitroarenes (1 mmol); TMSCl (2 mmol); n-Bu4NPF6 (0.04 mol); THF (50 mL); SmI2 (10 mol %); current intensity (0.05 A); 20 °C; 5 h).
Figure 19. Electrocatalytic reduction of nitrobenzene using SmI2 as electrode [92]. (The optimal reaction conditions: nitroarenes (1 mmol); TMSCl (2 mmol); n-Bu4NPF6 (0.04 mol); THF (50 mL); SmI2 (10 mol %); current intensity (0.05 A); 20 °C; 5 h).
Molecules 28 06741 g019
Molecules 28 06741 g020
Figure 20. Photochemical reduction of nitrobenzene catalyzed by Pd@CdS [93]. (The optimal reaction conditions: nitrosobenzene, (100 μmol); glucose (100 μmol); water (1 mL); Pd@ CdS (0.025 g with 2 wt% metal); visible light irradiation (λ > 420 nm); 25 °C; 1 h).
Figure 20. Photochemical reduction of nitrobenzene catalyzed by Pd@CdS [93]. (The optimal reaction conditions: nitrosobenzene, (100 μmol); glucose (100 μmol); water (1 mL); Pd@ CdS (0.025 g with 2 wt% metal); visible light irradiation (λ > 420 nm); 25 °C; 1 h).
Molecules 28 06741 g020
Molecules 28 06741 g021
Figure 21. Photocatalytic reduction of nitrobenzene catalyzed by the CQDs/ZnIn2S4 composite [94]. (The optimal reaction conditions: nitrobenzene (0.2 mmol); 3.0 wt% CQDs/ZnIn2S4 (10 mg); TEOA/MeOH/H2O (2:1:1, 2 mL); N2; NaOH (6 mL); LED irradiation; 13 h).
Figure 21. Photocatalytic reduction of nitrobenzene catalyzed by the CQDs/ZnIn2S4 composite [94]. (The optimal reaction conditions: nitrobenzene (0.2 mmol); 3.0 wt% CQDs/ZnIn2S4 (10 mg); TEOA/MeOH/H2O (2:1:1, 2 mL); N2; NaOH (6 mL); LED irradiation; 13 h).
Molecules 28 06741 g021
Molecules 28 06741 g022
Figure 22. Biosynthesis of azo compounds catalyzed by laccase. [95]. (The optimal reaction conditions: aromatic amines (5 mmol); pH (6); CotA laccase (1 UmL−1); O2; 37 °C).
Figure 22. Biosynthesis of azo compounds catalyzed by laccase. [95]. (The optimal reaction conditions: aromatic amines (5 mmol); pH (6); CotA laccase (1 UmL−1); O2; 37 °C).
Molecules 28 06741 g022
Molecules 28 06741 g023
Figure 23. Synthesis of azobenzene from aniline mediated by ethyl lactate [96]. (The optimal reaction conditions: aniline (1 mmol); oxone (0.5 mmol); ethyl lactate; room temperature; 90 °C; 12 h).
Figure 23. Synthesis of azobenzene from aniline mediated by ethyl lactate [96]. (The optimal reaction conditions: aniline (1 mmol); oxone (0.5 mmol); ethyl lactate; room temperature; 90 °C; 12 h).
Molecules 28 06741 g023
Molecules 28 06741 g024
Figure 24. Synthesis of azo compounds by hydrazine–halogen exchange [97]. (The optimal reaction conditions: N2H4·H2O (0.2 mmol), ([Ph-I-Mes]OTf (0.4 mmol), phthalic anhydride (1 mmol), CuI (10 mol %), and K2CO3 (2 mmol), DMF (2 mL), air).
Figure 24. Synthesis of azo compounds by hydrazine–halogen exchange [97]. (The optimal reaction conditions: N2H4·H2O (0.2 mmol), ([Ph-I-Mes]OTf (0.4 mmol), phthalic anhydride (1 mmol), CuI (10 mol %), and K2CO3 (2 mmol), DMF (2 mL), air).
Molecules 28 06741 g024
Molecules 28 06741 g025
Figure 25. Synthesis of asymmetric azo compounds by palladium-catalyzed C-N coupling [98]. (The optimal reaction conditions: N-aryl-N′-silyl diazenes (1.2 mmol); (dppf)PdCl2 (2 mol %); Cs2CO3 (1.3 mmol); toluene (0.2 mL); 60 °C; 15 h).
Figure 25. Synthesis of asymmetric azo compounds by palladium-catalyzed C-N coupling [98]. (The optimal reaction conditions: N-aryl-N′-silyl diazenes (1.2 mmol); (dppf)PdCl2 (2 mol %); Cs2CO3 (1.3 mmol); toluene (0.2 mL); 60 °C; 15 h).
Molecules 28 06741 g025
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Zhao, M.-Y.; Tang, Y.-F.; Han, G.-Z. Recent Advances in the Synthesis of Aromatic Azo Compounds. Molecules 2023, 28, 6741. https://doi.org/10.3390/molecules28186741

AMA Style

Zhao M-Y, Tang Y-F, Han G-Z. Recent Advances in the Synthesis of Aromatic Azo Compounds. Molecules. 2023; 28(18):6741. https://doi.org/10.3390/molecules28186741

Chicago/Turabian Style

Zhao, Meng-Yun, Yue-Feng Tang, and Guo-Zhi Han. 2023. "Recent Advances in the Synthesis of Aromatic Azo Compounds" Molecules 28, no. 18: 6741. https://doi.org/10.3390/molecules28186741

Article Metrics

Back to TopTop