β–α Photoisomerization of Cobaloxime Complexes in the Solid State. 5. Reaction Rate Reduced by a Hydrogen Bond

• Published in: Bulletin of the Chemical Society of Japan Vol. 69; no. 11; pp. 3107 - 3114
• Main Authors: Amano, Hiroki, Sekine, Akiko, Ohashi, Yuji, Hagiwara, Mieko, Sato, Junko, Arai, Yoshifusa, Ohgo, Yoshiaki
• Format: Journal Article
• Language: English
• Published: The Chemical Society of Japan 01.11.1996
• ISSN: 0009-2673; 1348-0634
• DOI: 10.1246/bcsj.69.3107

The crystal structures of three cobaloxime complexes with different axial base ligands have been analyzed by X-ray analysis at room temperature. I: (2-Cyanoethyl)bis(dimethylglyoximato)((S)-phenylalaninol)cobalt(III); the crystal is orthorhombic, the space group being P212121, Z = 4 with a = 9.416(3), b = 27.184(3), c = 9.184(3) Å. II: (2-Cyanoethyl)bis(dimethylglyoximato)((S)-phenyl-alanine methyl ester)cobalt(III); the crystal is monoclinic, the space group being P21, Z = 4 with a = 14.376(2), b = 11.988(2), c = 14.874(1) Å, and β = 101.05(1)°. III: (2-Cyanoethyl)bis(dimethylglyoximato)(methyldiphenylphosphine)cobalt(III); the crystal is monoclinic, the space group being P21/n, Z = 4 with a = 11.558(4), b = 15.542(3), c = 14.393(5) Å, and β = 91.02(4)°. The structures were refined by the full-matrix least-squares method to final R values of 0.041, 0.052, and 0.044 for 2340, 3287, and 4400 observed reflections, respectively. The photoisomerization rates of I, II, and III in the solid state were obtained from the changes in the IR spectra. The rate of I was insignificantly small, but the rates of II and III were calculated to be 0.1 × 10−4 and 1.9 × 10−4 s−1, respectively, assuming first-order kinetics. The 2-cyanoethyl groups in the three complex crystals take perpendicular conformations to their cobaloxime planes. The 2-cyanoethyl group of I makes a hydrogen bond with the N–H group of the neighboring molecule. The non-reactivity of I may be brought about by the hydrogen bond.