Issue 14, 2000

X-Ray diffraction and spectroscopic studies of the light-induced metastable state of a ethylenediamine nitrosyl ruthenium complex

Abstract

Blue-laser irradiation of a single crystal of the chloride salt of a cationic complex, trans-[Ru(en)2(H2O)(NO)]3+ (en = ethylenediamine), yielded MS1 (a metastable state of end-on type) which is remarkably stable (decay temperature Td = 267 K) compared with MS1 of sodium nitroprusside Na2[Fe(CN)5(NO)] (SNP). No MS2 state (side-on type) was observed by X-ray diffraction and IR spectroscopy. Even with a low population of 8% of the metastable species, the structure was clearly determined by X-ray analysis. For the first time, we observed an elongation of the N–O bond by X-ray diffraction, corresponding to a frequency downshift of the ν(NO) stretching vibration. The remarkably long lifetime of the metastable state of trans-[Ru(en)2(H2O)(NO)]3+ compared with that of SNP is explained by a stereochemical analysis using reaction cavity diagrams.

Supplementary files

Article information

Article type
Paper
Submitted
10 Feb 2000
Accepted
22 May 2000
First published
26 Jun 2000

J. Chem. Soc., Dalton Trans., 2000, 2425-2431

X-Ray diffraction and spectroscopic studies of the light-induced metastable state of a ethylenediamine nitrosyl ruthenium complex

M. Kawano, A. Ishikawa, Y. Morioka, H. Tomizawa, E. Miki and Y. Ohashi, J. Chem. Soc., Dalton Trans., 2000, 2425 DOI: 10.1039/B001132K

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