Submitted Successfully!
Thank you for your contribution! You can also upload a video entry related to this topic through the link below:
Check Note
Ver. Summary Created by Modification Content Size Created at Operation
1 + 3193 word(s) 3193 2021-12-08 04:30:23 |
2 format correction + 17 word(s) 3210 2021-12-15 04:25:38 |
Metal-Nitrosophenolato Complexes
Upload a video

Metal-nitrosophenolato complexes consist of a metal ion (most commonly copper(II)) flanked by typically two or more 2-nitrosophenolate ligands. The syntheses of them demonstrate a privileged introduction of a nitroso (and a hydroxyl via the Baudisch reaction) group to an aromatic ring. These complexes first appeared in the literature as early as 1939, and a range of applications has subsequently been published. However, optimisations of the preparative sequences were not considered, and as such, the reactions have seldom been utilised in recent years; indeed, there remains confusion in the literature as to how such complexes form.

  • C-nitrosation
  • copper complexes
  • Baudisch reaction
  • nitrosophenols
  • ortho-nitrosophenols
  • regioselective aromatic functionalisation
Subjects: Chemistry, Organic
Contributor :
View Times: 49
Entry Collection: Organic Synthesis
Revisions: 2 times (View History)
Update Time: 15 Dec 2021

1. Introduction to Metal-Nitrosophenolato Complexes

Metal-nitrosophenolato complexes consist of a metal ion (most commonly copper(II)) flanked by typically two or more 2-nitrosophenolate ligands. The structures of the nitrosophenols (both as ligands and free molecules) are known to resonate between the nitrosophenol and the quinone-monoxime forms [1][2][3]. Although the monoxime is considered to dominate, most literature representations display the nitrosophenol form, often for clarity and simplicity. Interestingly, the nitrosophenolato complexes are often highly coloured and reported to possess only limited solubility in most common organic solvents and water. Historically, the complexes have featured in a wide range of publications most often-based upon their colourimetric properties, although in recent years, both the metal complexes and their 2-nitrosophenol ligands have received little attention, becoming an almost forgotten class of molecules. However, one compound that has gained current commercial applicability [4] is an iron tris(1-nitroso-2-naphtholato), a dye known as ‘pigment green 8’ (Figure 1) [5][6][7]. This vivid green species has found widespread application in concrete, textiles, paint and rubber colouration.
Figure 1. The molecular structure of the commercially available dye, ‘Pigment green 8’ (aka ‘Pigment Green B’) [6].

2. Metal-Nitrosophenolato Complexes in Nature

Remarkably, substituted iron tris(nitrosophenolato) complexes are naturally biosynthesised by particular Streptomycete bacteria as specialised antibiotics [8][9][10][11]. Ferroverdin (Figure 2) was the first confirmed natural product to be isolated [8], although this was rapidly followed by the related Viridomycin A, Actinoviridin and Viridomycin E [12]. These complexes were found to target certain bacteria by disrupting their cell membranes; however, the free ligands were determined to be more effective than the corresponding iron complexes [13]. Interestingly, despite the presence of three negatively charged ligands, the complexes all exist in the Fe(II) oxidation state, with the overall negative charge counterbalanced with a sodium or equivalent cation [9][14]. It should, however, be acknowledged that this general characterisation is not universally accepted [12], and is complicated by the fact that the compounds are redox active and that, although the complexes are largely inert [13], ligands can be added/removed under a range of mild conditions [14]. Interestingly, these complexes were biosynthesised by the Streptomyces by incubation in a ferrous environment (e.g., with FeSO4) with carbon sources such as fructose and alanine in an assumingly complex pathway that is not extensively discussed [12], phosphate sources were also provided in most cases [11]. They were eventually identified as secondary metabolites and did not appear to assist in the regulatory uptake of iron into the cell [12]. The same iron complexes have now also been synthesised, using Cronheim’s copper-mediated nitrosation method (to be discussed in due course), followed by transmetallation to the ferrous complex [12][13][15].
Figure 2. The structures of four antibiotics isolated from Stroptomyces bacteria, Viridomycin A [13], Actinoverdin A, Ferroverdin [9] and Viridomycin E. Viridomycin E has been described in only a single publication [12] and could well exist preferentially as the hexadentate sodium salt, equivalent to the other 3 examples.

3. A Brief History of Metal-Nitrosophenolato Synthesis

The very first appearance of metal-nitrosophenolato complexes was reported by Eugéne Millon [16] in 1849, involving the formation of a mercury(II) complex. As indicated, such complexes are usually highly coloured, which inspired their continued preparation and isolation; indeed, the first fully isolated example appeared as early as 1900, but was originally misidentified as an ortho-nitrophenol complex of mercury with four pendant ligands [17]. It has now been comprehensively shown that this isolated compound was actually the corresponding mercuric-nitrosophenolato complex [18][19]. The analytical value of these intensely coloured complexes has over the years been widely exploited via the ‘Millon reagent’ or ‘Millon test’. This test has been used as a qualitative detection method for tyrosine, as well as other phenol functional molecules present in solution [14][17].
The next big development in the preparation of metal-nitrosophenolato compounds was realized by the Austrian chemist, Oskar Baudisch, during the early part of last century [20][21]. The developed synthesis represents a very interesting and novel functionalisation of an aromatic ring (such as benzene), where a hydroxy and nitroso moiety are added with defined ortho-regioselectivity. The functional aromatics are formed in the presence of a metal ion, typically copper(I) or (II) and hence post reaction, the compounds remain co-ordinated to the metal, forming a stable dimeric complex (in the case of copper). Advances in the fundamental understanding of this sequence, which has become known as the ‘Baudisch reaction’, including its underlying mechanism, have been explored in several publications, but the experimental results and conclusions have never been reviewed in a comprehensive fashion, and despite multiple recent advances in copper-mediated nitrosation procedures [22][23], the related Baudisch scheme has been neglected.

4. Introduction to the Baudisch Reaction

While not being a commonly encountered or formally recognised named reaction, the term ‘Baudisch reaction’ has become synonymous with specific processes that synthesise metal-nitrosophenolato compounds. In the original reported work, Baudisch employed a range of copper(I) and (II) sources and ‘Merck’s Superoxol’ (historic, commercial name for aqueous hydrogen peroxide) with benzene [20][21]. In addition, either hydroxylamine or a nitrous acid source was further supplied to introduce the corresponding nitroso moiety, hence forming complexes as the end product (Scheme 1 and Scheme 2). Baudisch in his reports proposed that the mechanism was much the same whether hydroxylamine or a nitrite source was used, although findings from later publications to be discussed cast significant doubts over this conclusion.
Scheme 1. Five different reactions (1–5) that Baudisch chose to publish, across two publications, which have subsequently become known as the Baudisch reaction [20][21]. aBaudisch states in the literature that ‘freshly prepared yellow cuprous hydroxide’ was used; it is known that this is not a stable entity, so the actual active substance could well be an alternative such as cuprous oxide, Cu2O.
Scheme 2. A clear distinction between copper-mediated aromatic nitrosation of phenols and the Baudisch conditions is demonstrated by the reporting of a different major product from the same starting material (3) [15][26].

6. Additional Syntheses of Metal-Nitrosophenolato Complexes

A further alternative synthetic approach would be to generate the free 2-nitrosophenol compounds first and then react them in a secondary process with a metal salt (e.g., copper(II) chloride). A copper ion, for example, will readily combine with 2-nitrosophenol under a range of monophasic or biphasic solvent systems, due to the substantial binding affinity [1][15][27]. Indeed, the thermodynamic stability of the copper-nitrosophenolato complexes is such that the biphasic reaction of a ligand in an organic solvent with a copper(II) salt in water is often completed quantitatively in only a few minutes [15]. Free 2-nitrosophenols can be made by partial oxidation of 2-aminophenols, in some cases [28], as well as a simple C-nitrosation of a phenol [27][29][30][31]. The scope of this particular approach however appears limited to certain 5-substituted-2-nitrosophenols and ortho nitrosonaphthols [1][31][32].
In contrast, the ligands can be freed from the complexes through the action of a strong acid. These reactions were demonstrated by Cronheim to show the formation and decomplexation of these complexes, as visualised by substantial colourimetric differences. The recovered yields for the free ligands were not reported; but Cronheim described ‘relatively low yields’, which is expected due to the nitrosophenol compounds’ strong ligand binding affinity and the temperamental acid-stability of the free ligands. A much improved technique allowing simple isolation of the 2-nitrosophenol involves the use of a copper-scavenger, which coordinates with a higher binding affinity and thus selectively displaces the chelating nitrosophenol ligands [24].
The ligand-metal association method is not as applicable as might first be expected due to problems with isolating the free 2-nitrosophenol compounds. Indeed, there are only very limited experimental procedures documenting the preparation and isolation of 2-nitrosophenols. It is a common misconception that C-nitrosation of phenols predominantly produce the corresponding 2-nitrosophenol regioisomer, as per the general expectation for an SEAr process [29][33][34]. Conversely, unless there is a blocking group at the 4-position or a very strongly directing or bulky group at the 3-position, nitrosation of phenols occurs almost exclusively para to the hydroxyl group [35]. This occurs because even though the 2-nitrosophenol is the kinetic product, owing to the ability of the nitroso group to undergo migration to a more favourable position of the Wheland intermediate, the thermodynamic 4-substitued product is almost the sole isolated adduct [2][36]. It should also be noted that examples of 4-substituted-2-nitrosophenols are still relatively rare and mainly historical, the one recent publication [37] describing the preparation, isolation and characterisation of four such compounds has since been retracted, hence the existence of these compounds remains unconfirmed. Electronics also play an important role as aromatics with electron-withdrawing substituents are generally inert to nitrosation (hence why poly nitrosation is rarely observed), to a greater extent even than nitration [38], with toluene being about the least electron-rich aromatic known to undergo C-nitrosation [28][32][34].
This preference for para-nitrosation is seemingly altered in the Baudisch conditions where the formation of a complex stabilises the 2-nitrosophenol ligand against rearrangement. Complexation also helps prevent condensation/decomposition or oxidation to the nitro derivative [18][36], factors which likely explain why free 2-nitrosophenol compounds are so rarely reported and characterised in the literature. Despite their highly reactive nature, a small collection of publications describe the synthesis and isolation of 2-nitrosophenols possessing a meta substituent, rather than a para ‘blocking’ group (Scheme 3) [31][39][40]. In each case, the metal substituent was a π-donor comparable in strength to or exceeding the phenol directing group, hence attenuating the natural preference for para-nitrosation relative to the phenol.
Scheme 3. Three literature procedures for the successful synthesis, isolation and characterisation of 3-substituted-2-nitrosophenols [39][40]. Yields refer to pure, isolated compounds.
Consequently, not all metal-nitrosophenolato complexes can be formed when metal salts are combined with free 2-nitrosophenols [41]. Several failed attempts to synthesise complexes have been reported [1]; however, investigating the experimental approach it is not clear if this was as a result of complex instability or actually unsuccessful synthesis of the ligand in the first place. In general, there are four principal synthesis routes to the discussed complexes, and although their preparations can be problematic, the corresponding complexes can often be readily obtained by simple precipitation. Some representative reaction conditions are summarised in Table 1 and will be discussed further in more detail subsequently.
Table 1. General conditions reported to produce metal-nitrosophenolato complexes, highlighting a representative copper example for each case.


Accepted Starting Materials

Baudisch conditions with hydroxylamine

A range of aromatics including benzene, phenols, catechols, naphthalenes and phenylsulfinic acids [20][42][43].

Molecules 24 04018 i001

Baudisch conditions with nitrous acid

Shown to accept benzene. Similar aromatics expected to work, though scope not investigated [20].

Molecules 24 04018 i002

Copper-mediated aromatic nitrosation

Phenols with sufficiently electron-rich aromatic ring and at least one non-functionalised carbon atom ortho to the phenol [15][41].

Molecules 24 04018 i003

Association of free 2-nitrosophenols with copper

STable 2-nitrosophenol compounds [1][15][41].

Molecules 24 04018 i004

All experiments can be conducted at room temperature.

7. Scope of Metal-Nitrosophenolato Synthesis

While the mechanism of the Baudisch reaction implies that almost any aromatic should be able to form a copper-nitrosophenolato complex, in practice, the Baudisch conditions have not been extensively investigated for their scope. More commonly, this approach has been relegated in favour of either the copper (or other metal)-mediated phenol nitrosation procedure or the direct complexation of the free-ligand with a metal salt (it is worth noting that these latter schemes are still often unhelpfully referred to as the ‘Baudisch reaction’). For this reason, there is often a strong correlation between the number of available literature references for a given nitrosophenol ligand and that of the related metal complex. The exception is for 4-substituted-2-nitrosophenols, such as 4-chloro-2-nitrosophenol, where there has been no reliable confirmation of existence for the free ligand, whereas the corresponding metal complex has been repeatedly reported. The sub-class of o-nitrosonaphthols appears to form the most popular complexes, probably because several o-nitrosonaphthols are more stable and are also commercially available [44]. A range of metals have thus been utilised in their complexation. Historically, these were initially smaller, first-row transition metals, though larger metals have subsequently been found to form complexes too, including (but not limited to) gold [15], palladium [45], ruthenium [46] and more recently even samarium [47].

8. Properties of Metal-2-Nitrosophenolato Complexes

One of the first publications highlighting the properties of a vast assortment of metal-nitrosophenolato complexes came from German chemist, Georg Cronheim [15], whose team prepared and analysed over 50 different complexes. It was also suggested in this seminal publication that the free 2-nitrosophenol ligands were isolated from these complexes; however, yields, purities, stabilities or structural data were not provided to support this statement. It was found that stable complexes formed with a variety of metal +2 centres, especially mercury(II), nickel(II), iron(II), cobalt(II) and palladium(II). Other metals in different oxidation states, including silver(I) and gold(III) were also found to have affinity for the free 2-nitrosophenols. Interestingly, if insufficient free nitrosophenol was present for complete conversion to the bis-ligated complexes, mono-ligated complexes were selectively formed. These could be easily distinguished by their different solubilities, because the bi-ligated complexes were organic soluble but not aqueous, and the reverse was true for the mono-ligated. The majority of the complexes reported were prepared using Baudisch conditions; however, as 4-substitued-2-nitrosophenolato complexes cannot be made in this way, they were instead generated using what appears to be the first record of a copper-mediated nitrosation of phenols procedure (excluding examples of the Millon test [16]).
A later study, by Charalambous et al. [1], investigated the properties of additional metal-2-nitrosophenolato complexes and addressed some of the common misconceptions made in the earlier literature. Using infrared spectroscopy, it was discovered that the nitrosophenol ligands readily tautomerise to the more favoured o-benzoquinone monoxime structure (Figure 3), and the same is true for the free nitrosophenols [29].
Figure 3. The possible tautomers of copper(II) bis(4-methyl-2-nitrosophenol), (2b, 2bi).
It was not possible at the time to determine whether the metal atom coordinated to the nitrogen or the oxygen atom of the nitroso group. It has now been confirmed using single crystal X-ray diffraction (XRD) analysis that coordination is through the nitrogen (Figure 4) [29][48]. A Jahn-Teller distorted octahedral geometry is adopted, with the two aromatic ligands forming an equatorial plane and the axial positions occupied due to oligomerisation, with the phenolic oxygen typically as the donor, although its distance is a little outside the primary coordination sphere of the copper and instead within the Van der Waal’s radii [49]. This structure occurs for only completely dried, anhydrous compounds, otherwise a water (or another solvate, e.g., ethanol) is found sitting at the apex of the structure in the place of a neighbouring phenol oxygen. Almost all other published structures (where two nitrosophenolato ligands are present, with a single additional small donor) share the back-to-back square-based pyramid geometry, apart from one example, which reports a distorted trigonal bipyramid [50].
Figure 4. The unit cell of the obtained crystal structure of copper(II) bis(4-methyl-2-nitrosophenol) with ethanol as a solvate [41][51].
In all cases studied, when the copper complex is prepared the system tends to adopt a bi-ligated dimer unit as a maximum whereas other metals, such as the higher oxidation states of cobalt(III) or the larger iron (II or III) ions have been known to accommodate an additional nitrosophenol ligand, i.e., retaining an octahedral hexacoordinate structure bearing 3 ligands (Figure 5) [52] (although with nitrosophenols bearing larger substituents, e.g., 4-bromo-2-nitrosophenol, complexes remain bis-ligated, at least with Co(III)) [53]. These findings were fully supported by elemental analysis and UV-VIS absorbance data and proved at the time most revealing as up to this stage all complexes were assumed to be limited to just one or two nitrosophenol ligands [3][43].
Figure 5. The suggested structure of Cobalt(III) tris(4-methyl-2-nitrosophenolato) (5a) as specified in the publication by Mahmoud et al. and tautomeric forms (5b,c) indicating potential hydrogen bond donor sites [54].

9. Derivatisation of Complexes

While the organic nitrosophenolato ligands have enormous affinity for small metallic ions, like Cu(II), researchers have been able to derivatise the complexes with additional, neutral ligands. Cronheim first used pyridine as an auxiliary ligand to alter complex solubility [15], noting that the new compounds could be formed by simply mixing the copper (or other metal) nitrosophenolato complex with pyridine. Castellani et al. also synthesised several new complexes with additional neutral amine bases, again by simply stirring the parent complex at room temperature in acetonitrile, with a slight excess of the Lewis base (L, 6af, Table 2) [55]. Later, it was discovered that 6-coordinate complexes could be generated by additionally heating the complex with three equivalents of imidazole or N-methylimidazole in refluxing acetonitrile (6g,h, Table 2) [50] in order to overcome the interaction of the copper centre with a neighbouring phenolic oxygen atom. Other notable derivatisations recorded include the synthesis of a potassium (µ-iodo) copper nitrosophenolato complex, which comprises copper in both its octahedral and square-based pyramid geometries, bound by two bridging iodides (6i, Table 2) [56].
Table 2. A range of derivatised complexes generated by Castellani and co-workers, starting from copper bis(4-chloro-2-nitrosophenolato) with amine Lewis bases [55][56].

Molecules 24 04018 i005

Molecules 24 04018 i006

1 supported by elemental analysis data. 2 supported by a solved crystal structure from XRD analysis [55][56] as well as elemental analysis data. 3 synthesised by refluxing starting complex with 3 equiv. of ligand in MeCN rather than by stated scheme.
The complexes have also been shown to undergo transmetalations. Tamura et al. [18] report the conversion of mercury bis(4-methyl-2-nitrosophenolato) to the corresponding copper bis(4-methyl- 2-nitrosophenolato) in the presence of a simple copper salt (CuSO4). Remarkably, Charalambous, Castellani and co-workers have been able to synthesise and characterise crystalline nitrosophenolato complexes prepared from alkaline metals, i.e., sodium and lithium, by reacting with sodium and lithium hydroxide respectively [57]. Due to the redox characteristics of the ligands, these may have interesting properties for areas such as energy storage and battery materials [58].

10. Conclusion

The challenges in synthesis, lack of profusion in literature and unique properties of 2-nitrosophenols and their metal salts make them a stimulating target for further study. Across several publications, greater understanding has developed about their properties and the mechanisms to their formation. Applications are demonstrated, but not yet developed—the speciality of the process may afford application in the future. Doubts over specific aspects of the mechanisms proposed remain, and further study and characterisation of the structures proposed would aid in the understanding of the field. A publication [41], completed by our group, represents the initial stages of such as study.


  1. Charalambous, J.; Frazer, M.J.; Taylor, F.B. Complexes of copper(II) with o-nitrosophenols (monoximes of ortho-benzoquinones). J. Chem. Soc. A Inorg. Phys. Theor. 1969, 2787.
  2. Al-Obaidi, U.; Moodie, R.B. The nitrous acid-catalysed nitration of phenol. J. Chem. Soc. Perkin Trans. 2 1985, 467.
  3. Hayton, T.W.; Legzdins, P.; Sharp, W.B. Coordination and Organometallic Chemistry of Metal − NO Complexes. Chem. Rev. 2002, 102, 935–991.
  4. Zhang, M. Production Device of Rubber Colorant Pigment Green B 2017. Available online: (accessed on 28 July 2019).
  5. Wegener, J.W.; Klamer, J.C.; Govers, H.; Brinkman, U.A.T. Determination of organic colorants in cosmetic products by high-performance liquid chromatography. Chromatographia 1987, 24, 865–875.
  6. American Association of Textile Chemists and Colorists (AATCC). Available online: (accessed on 5 November 2019).
  7. Shi, H.; Zhang, T.; An, T.; Li, B.; Wang, X. Photocatalytic Hydroxylation of Phenol to Catechol and Hydroquinone by Using Organic Pigment as Selective Photocatalyst. Curr. Org. Chem. 2012, 16, 3002–3007.
  8. Chain, E.B.; Tonolo, A.; Carilli, A. Ferroverdin, a Green Pigment containing Iron produced by a Streptomycete. Nature 1955, 176, 645.
  9. Candeloro, S.; Grdenic, D.; Taylor, N.; Thompson, B.; Viswamitra, M.; Hodgkin, D.C. Structure of Ferroverdin. Nature 1969, 224, 589–591.
  10. Maciejewska, M.; Pessi, I.S.; Arguelles-Arias, A.; Noirfalise, P.; Luis, G.; Ongena, M.; Barton, H.; Carnol, M.; Rigali, S. Streptomyces lunaelactis sp. nov., a novel ferroverdin A-producing Streptomyces species isolated from a moonmilk speleothem. Antonie Van Leeuwenhoek 2015, 107, 519–531.
  11. Tomoda, H.; Tabata, N.; Shinose, M.; Takahashi, Y.; Woodruff, H.B.; Omura, S. Ferroverdins, Inhibitors of Cholesteryl Ester Transfer Protein Produccd by Streptomyces sp. WK-5344. I. Production, Isolation and Biological Properties. J. Antibiot. (Tokyo) 1999, 52, 1101–1107.
  12. KUROBANE, I.; DALE, P.L.; VINING, L.C. Characterization of new viridomycins and requirements for production in cultures of Streptomyces griseus. J. Antibiot. (Tokyo) 1987, 40, 1131–1139.
  13. Yang, C.C.; Leong, J. Mode of antibiotic action of 4-hydroxy-3-nitrosobenzaldehyde from Streptomyces viridans. Antimicrob. Agents Chemother. 1981, 20, 558–562.
  14. Basu, P.; Pal, S.; Chakravorty, A. Redox in a ferroverdin analogue: Recognition of isomeric co-ordination spheres by Fe II and Fe III. J. Chem. Soc. Chem. Commun. 1989, 977.
  15. Cronheim, G. O-Nitrosophenols. J. Org. Chem. 1947, 12, 1–29.
  16. Millon, E. Sur un Réacrif Propre aux composés proteiques. Compt. Rend. Acad. 1849, 132, 156.
  17. Vaubel, W. Zur Kenntniss der Millon’schen Reaction. Zeitschrift für Angew. Chemie 1900, 13, 1125–1130.
  18. Kido, Y.; Tamura, Z. An improved method for the millon reaction. Chem. Pharm. Bull. (Tokyo) 1981, 29, 2296–2302.
  19. Gibbs, H.D. PHENOL TESTS.* II. Nitrous Acid Tests. The Millon and Similar Spectrophotometric Iinvestigations. J. Biol. Chem. 1926, 71, 445–459.
  20. Baudisch, O. A New Chemical Reaction With the Nitrosyl Radical Noh. Science 1940, 92, 336–337.
  21. Baudisch, O.; Smith, S. Ftir die kurzen Originalmitteilungen ist ausschlieBlich der Verfasser verantwortlich. Kurze Orig. 1939, 17, 768–769.
  22. Deka, H.; Ghosh, S.; Gogoi, K.; Saha, S.; Mondal, B. Nitric Oxide Reactivity of a Cu(II) Complex of an Imidazole-Based Ligand: Aromatic C-Nitrosation Followed by the Formation of N-Nitrosohydroxylaminato Complex. Inorg. Chem. 2017, 56, 5034–5040.
  23. Kundu, S.; Kim, W.Y.; Bertke, J.A.; Warren, T.H. Copper(II) activation of nitrite: Nitrosation of nucleophiles and generation of NO by thiols. J. Am. Chem. Soc. 2017, 139, 1045–1048.
  24. Cone, M.C.; Melville, C.R.; Carney, J.R.; Gore, M.P.; Gould, S.J. 4-Hydroxy-3-nitrosobenzamide and its ferrous chelate from Streptomyces murayamaensis. Tetrahedron 1995, 51, 3095–3102.
  25. Dessouky, Y.M.; Gal El Rub, L.N. Colorimetric determination of procaine hydrochloride in pharmaceutical preparations. Analyst 1976, 101, 717–719.
  26. Maruyama, K.; Goto, R.; Tanimoto, I. Studies on the Baudisch Reaction. I. The Synthesis of O-Nitrosophenols. J. Org. Chem. 1967, 32, 2516–2520.
  27. Masoud, M.S.; Hindawey, A.M.; Mostafa, M.A.; Ramadan, A.M. Synthesis and structural chemistry of 2,4-dinitrosoresorcionl, 1-nitroso-2-naphthol and 4-carboxy-2-nitrosophenol. Spectrosc. Lett. 1997, 30, 1227–1247.
  28. Porta, F.; Prati, L. Catalytic synthesis of C-nitroso compounds by cis-Mo(O)2(acac)2. J. Mol. Catal. A Chem. 2000, 157, 123–129.
  29. Williams, D.L.H. Nitrosation Reactions and the Chemistry of Nitric Oxide, 1st ed.; Elsevier B.V: Bodmin, UK, 2004.
  30. Baluch, D.; Charalambous, J.; Haines, L.I.B. Manganese Complexes of 1,2-Naphthoquinone Mono-oximes (2-Nitrosophenols) as Catalysts for Alkene Epoxidation Dosten. J. Chem. Soc. Chem. Commun. 1988, 1178–1179.
  31. Aljaar, N.; Malakar, C.C.; Conrad, J.; Beifuss, U. Base-Promoted Domino Reaction of 5-Substituted 2-Nitrosophenols with Bromomethyl Aryl Ketones: A Transition-Metal-Free Approach to 2-Aroylbenzoxazoles. J. Org. Chem. 2015, 80, 10829–10837.
  32. Li, H.; Pang, M.; Wu, B.; Meng, J. Synthesis, crystal structure and photochromism of a novel spirooxazine derivative. J. Mol. Struct. 2015, 1087, 23–29.
  33. Atherton, J.H.; Moodie, R.B.; Noble, D.R. Kinetics and mechanism of nitrosation of toluene, o-xylene, and m-xylene in trifluoroacetic acid, or in acetic–sulfuric acid mixtures, under nitric oxide. J. Chem. Soc. Perkin Trans. 2 1999, 699–706.
  34. Leis, J.R.; Ríos, A.; Rodríguez-Sánchez, L. Reactivity of phenolic nucleophiles towards nitroso compounds. Part 2.1 Reaction with alkyl nitrites (O-nitroso compounds). J. Chem. Soc. Perkin Trans. 2 1998, 2729–2734.
  35. Charalambous, J.; Kensett, M.J.; Jenkins, J.M. Deoxygenation of 2-nitrosophenols and of their metal complexes with triphenylphosphine. Synthesis of phenazines, dihydrophenazines, triphenyl(o-hydroxyphenylimino)phosphoranes and their metal complexes. J. Chem. Soc. Chem. Commun. 1977, 400–401.
  36. Atherton, J.H.; Moodie, R.B.; Noble, D.R.; O’Sullivan, B. Nitrosation of m-xylene, anisole, 4-nitrophenyl phenyl ether and toluene in trifluoroacetic acid or in acetic–sulfuric acid mixtures under nitric oxide. J. Chem. Soc. Perkin Trans. 2 1997, 2, 663–664.
  37. Ramozzi, R.; Chéron, N.; El Kaïm, L.; Grimaud, L.; Fleurat-Lessard, P. Predicting new ugi-smiles couplings: A combined experimental and theoretical study. Chem.-A Eur. J. 2014, 20, 9094–9099.
  38. Bosch, E.; Kochi, J.K. Direct Nitrosation of Aromatic Hydrocarbons and Ethers with the Electrophilic Nitrosonium Cation. J. Org. Chem. 1994, 59, 5573–5586.
  39. Crossley, M.L.; Dreisbach, P.F.; Hofmann, C.M.; Parker, R.P. Chemotherapeutic Dyes. I. 5-Aralkylamino-9-alkylaminobenzo phenoxazines 1. J. Am. Chem. Soc. 1952, 74, 573–578.
  40. Maleski, R.J.; Kluge, M.; Sicker, D. A facile access to substituted 2-nitrosophenols and 2-nitrophenols via regioselective nitrosation of resorcinol monoethers. Synth. Commun. 1995, 25, 2327–2335.
  41. Nicholls, A.J.; Batsanov, A.S.; Baxendale, I.R. Copper-Mediated Nitrosation: 2-Nitrosophenolato Complexes and their use in the Synthesis of Heterocycles. Molecules 2019. under review.
  42. Maruyama, K.; Tanimoto, I. Studies on the Baudisch Reaction. IV. The Reaction Mechanism. Bull. Chem. Soc. Jpn. 1971, 44, 3120–3123.
  43. Konecny, J.O. Hydroxylation of Benzene in Aqueous Solution in the Presence of Hydroxylamine Hydrochloride. J. Am. Chem. Soc. 1955, 77, 5748–5750.
  44. 1-Nitroso-2-Naphthol (2019). Available online: (accessed on 1 August 2019).
  45. Patil, S.V.; Mohite, B.S. Palladium (II) Chelates of some o-Nitrosophenols. J. Mol. Catal. 1977, 46, 638.
  46. Ka-Hong Lee, K.; Wong, W.-T. Syntheses and molecular structures of ruthenium carbonyl complexes containing 1,2-naphthoquinone-1-oximate ligands. J. Chem. Soc. Dalt. Trans. 1997, 2987–2996.
  47. Lyubchenko, S.N.; Ionov, A.M.; Shcherbakov, I.N.; Aleksandrov, G.G.; Kogan, V.A.; Tsivadze, A.Y. Coordination compounds based on 4,6-di-tert-butyl-2-nitrosophenol. Russ. J. Coord. Chem. 2006, 32, 539–544.
  48. Rout, K.C.; Mondal, B. Aromatic C-nitrosation by a copper(ii)–nitrosyl complex. Dalt. Trans. 2015, 44, 1829–1835.
  49. Baluch, D. Studies of 1,2-Quinone Mono-Oximato Complexes and Their Redox Reactions; The Polytechnic of North London: London, UK, 1987. Available online: (accessed on 5 November 2019).
  50. Castellani, C.B.; Carugo, O. Studies on copper(II) complexes of o-quinone monooximes. 8. Penta and hexacoordinated adducts of bis(4-chloro-1,2-benzaquinone 2-oximato)copper(II), , with imidazole and N-methylimidazole. Inorg. Chim. Acta 1988, 150, 119–123.
  51. The Cambridge Crystallographic Data Centre Home—The Cambridge Crystallographic Data Centre (CCDC). Available online: (accessed on 5 November 2019).
  52. Basu, P. Cobalt analogue of ferroverdin: Synthesis and geometric structure. Polyhedron 1992, 11, 3037–3040.
  53. Castellani, C.B.; Buttafava, A.; Carugo, O.; Poggi, A. Studies on metal complexes of ortho-quinone mono-oximes. Part 6. Redox behaviour of bis(4-chloro-1,2-benzoquinone 2-oximato)-copper(II) and -nickel(II); synthesis and characterization of reduced species containing a paramagnetic ligand. J. Chem. Soc. Dalt. Trans. 1988, 1497.
  54. Masoud, M.S.; Haggag, S.S.; Ramadan, A.M.; Mahmoud, S. a Nitrosophenol complexes of transition metal salts. Transit. Met. Chem. 1998, 23, 343–347.
  55. Castellani, C.B.; Gatti, G.; Millini, R. Studies on copper(II) Complexes of o-quinone monooximes. adducts of bis(4-chioro-1 -benzoquinone 2-oximato) copper(II) with Some heterocyclic bases. structure of the 2,2’-bipyridine adduct. Inorg. Chem. 1984, 23, 4004–4008.
  56. Castellani, C.B.; Carugo, O.; Coda, A. Studies on copper(II) complexes of o-quinone monooximes. 3. Reactivity of bis(4-chloro-1-benzoquinone 2-oximato)copper(II) with halides. Crystal structure of potassium bis(.mu.-iodo)tris. Inorg. Chem. 1987, 26, 671–675.
  57. Adatia, T.; Chakrabarti, J.; Charalambous, J.; Carugo, O.; Castellani, C.B. Synthesis and structural characterization of lithium and sodium complexes of 5-ethylamino-4-methyl-1,2-benzoquinone 2-oxime. Polyhedron 1996, 15, 1331–1338.
  58. Li, F.; Liu, Q.; Hu, J.; Feng, Y.; He, P.; Ma, J. Recent advances in cathode materials for rechargeable lithium–sulfur batteries. Nanoscale 2019, 11, 15418–15439.
Subjects: Chemistry, Organic
Contributor :
View Times: 49
Entry Collection: Organic Synthesis
Revisions: 2 times (View History)
Update Time: 15 Dec 2021
Table of Contents


    Are you sure to Delete?

    Video Upload Options

    Do you have a full video?
    If you have any further questions, please contact Encyclopedia Editorial Office.
    Nicholls, A. Metal-Nitrosophenolato Complexes. Encyclopedia. Available online: (accessed on 04 July 2022).
    Nicholls A. Metal-Nitrosophenolato Complexes. Encyclopedia. Available at: Accessed July 04, 2022.
    Nicholls, Alexander. "Metal-Nitrosophenolato Complexes," Encyclopedia, (accessed July 04, 2022).
    Nicholls, A. (2021, December 14). Metal-Nitrosophenolato Complexes. In Encyclopedia.
    Nicholls, Alexander. ''Metal-Nitrosophenolato Complexes.'' Encyclopedia. Web. 14 December, 2021.