Transition metal nitroso complexes

Transition metal nitroso complexes are coordination complexes containing one or more organonitroso ligands (RNO).^[1]

Structure and bonding edit

Structure of the dye Naphthol Green B, which features of nitroso ligand bound to Fe(III).

Organic nitroso compounds bind to metals in several ways, but most commonly as monodentate N-bonded ligands. Also known are O-bonded, η²-N,O-bonded. Dimers of organic nitroso compounds also bind in a κ²--O,O bidentate manner.

Synthesis edit

Organic nitroso complexes can be prepared from preformed organic nitroso precursors. These precursors usually exist as N-N bonded dimers, but the dimer dissociates readily. This direct method is used to give W(CO)₅(tert-BuNO) (where tert-Bu is (CH₃)₃C).^[2] The Fe-porphyrin complex depicted below is prepared by this route. More complicated but more biorelevant routes involve degradation of precursors such as nitrobenzene and phenylhydroxylamine.^[3]

Ni(PEt₃)₄ + i−PrNO₂ → Ni(PEt₃)₂(η²-i−PrNO) + PEt₃ + OPEt₃ (Et = C₂H₅, i-Pr = (CH₃)₂CH)

The coupling of organic ligands and nitric oxide is yet another route.^[1]

Connection to methemoglobinemia edit

Structure of Fe(octaethylporphyrin)(C₆H₅NO)(imidazole). This synthetic complex is thought to resemble heme inhibited by nitroso benzene. Color code: red = O, blue = N, Fe, gray = C, white = H.

Methemoglobinemia is a disorder where a large fraction of hemoglobin in one's blood has converted to inactive forms, generically called methemoglobin. Since methemoglobin is not an oxygen-carrier, methemoglobinemia is a serious disorder, sometimes fatal. Exposure to nitrobenzene, aniline, and their derivatives cause this disorder, which is attributed to their conversion to nitrosobenzene (and derivatives), which inactivate hemoglobin by forming a complex with the Fe center, precluding binding of O₂.^[4]

References edit

^ ^a ^b Lee, Jonghyuk; Chen, Li; West, Ann H.; Richter-Addo, George B. (2002). "Interactions of Organic Nitroso Compounds with Metals". Chemical Reviews. 102 (4): 1019–1066. doi:10.1021/cr0000731. PMID 11942786.
^ Pilato, R. S.; McGettigan, C.; Geoffroy, G. L.; Rheingold, A. L.; Geib, S. J. (1990). "tert-Butylnitroso Complexes. Structural Characterization of W(CO)₅(N(O)Bu-tert) and [CpFe(CO)(PPh₃)(N(O)Bu-tert)]⁺". Organometallics. 9 (2): 312–17. doi:10.1021/om00116a004.
^ Berman, R. S.; Kochi, J. K. (1980). "Kinetics and Mechanism of Oxygen Atom Transfer from Nitro Compounds Mediated by Nickel(0) Complexes". Inorganic Chemistry. 19: 248–254. doi:10.1021/ic50203a050.
^ Godbout, Nathalie; Sanders, Lori K.; Salzmann, Renzo; Havlin, Robert H.; Wojdelski, Mark; Oldfield, Eric (1999). "Solid-State NMR, Mössbauer, Crystallographic, and Density Functional Theory Investigation of Fe−O₂and Fe−O₂Analogue Metalloporphyrins and Metalloproteins". Journal of the American Chemical Society. 121 (16): 3829–3844. doi:10.1021/ja9832820.

[GBRA-1] Lee, Jonghyuk; Chen, Li; West, Ann H.; Richter-Addo, George B. (2002). "Interactions of Organic Nitroso Compounds with Metals". Chemical Reviews. 102 (4): 1019–1066. doi:10.1021/cr0000731. PMID 11942786.

[2] Pilato, R. S.; McGettigan, C.; Geoffroy, G. L.; Rheingold, A. L.; Geib, S. J. (1990). "tert-Butylnitroso Complexes. Structural Characterization of W(CO)₅(N(O)Bu-tert) and [CpFe(CO)(PPh₃)(N(O)Bu-tert)]⁺". Organometallics. 9 (2): 312–17. doi:10.1021/om00116a004.

[3] Berman, R. S.; Kochi, J. K. (1980). "Kinetics and Mechanism of Oxygen Atom Transfer from Nitro Compounds Mediated by Nickel(0) Complexes". Inorganic Chemistry. 19: 248–254. doi:10.1021/ic50203a050.

[4] Godbout, Nathalie; Sanders, Lori K.; Salzmann, Renzo; Havlin, Robert H.; Wojdelski, Mark; Oldfield, Eric (1999). "Solid-State NMR, Mössbauer, Crystallographic, and Density Functional Theory Investigation of Fe−O₂and Fe−O₂Analogue Metalloporphyrins and Metalloproteins". Journal of the American Chemical Society. 121 (16): 3829–3844. doi:10.1021/ja9832820.

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