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N-Methylhydroxylamido(1−)- and Nitrosomethaneruthenium Complexes Derived from Nitrosyl Complexes: Reversible N-Protonation of an N-Coordinated Nitrosoalkane

✍ Scribed by Satoshi Kura; Shigeki Kuwata; Takao Ikariya


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
126 KB
Volume
44
Category
Article
ISSN
0044-8249

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✦ Synopsis


Nitric oxide (NO), nitroxyl (HNO), and hydroxylamine have been invoked as key intermediates in the biological multielectron reduction of nitrite to ammonia, which is a fundamental process in the inorganic nitrogen cycle in nature. The reaction is catalyzed by a certain type of nitrite reductase that contains heme moieties at its active site.


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## Abstract Reaction of (__R__)‐bis(pyrrol‐2‐ylmethyleneamino)‐1,1′‐binaphthyl (1H~2~) or (__R__)‐__N__,__N′__‐bis(pyridin‐2‐ylmethyl)‐1,1′‐binaphthyl‐2,2′‐diamine (2H~2~) with Zr(NMe~2~)~4~ (1 equiv.) gives chiral zirconium amides 1‐Zr(NMe~2~)~2~·C~7~H~8~ (4·C~7~H~8~) or 2‐Zr(NMe~2~)~2~ (6) in goo