LASER FLASH-PHOTOLYSIS STUDIES OF NITRITOMANGANESE(III) TETRAPHENYLPORPHYRIN - REACTIONS OF O-2, NO, AND PYRIDINE WITH MANGANESE(II) TETRAPHENYLPORPHYRIN

Citation
M. Hoshino et al., LASER FLASH-PHOTOLYSIS STUDIES OF NITRITOMANGANESE(III) TETRAPHENYLPORPHYRIN - REACTIONS OF O-2, NO, AND PYRIDINE WITH MANGANESE(II) TETRAPHENYLPORPHYRIN, Inorganic chemistry, 37(10), 1998, pp. 2464-2469
Citations number
52
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
37
Issue
10
Year of publication
1998
Pages
2464 - 2469
Database
ISI
SICI code
0020-1669(1998)37:10<2464:LFSONT>2.0.ZU;2-9
Abstract
Laser photolysis of nitritomanganese(III) tetraphenylporphyrin, (MnTPP )-T-III(ONO) (1), in degassed toluene gives manganese(II) tetraphenylp orphyrin, (MnTPP)-T-III (2), plus NO2. The quantum yield, Phi, for the formation of (MnTPP)-T-II is dependent on the excitation wavelength: Phi = 0.045 at 355nm and Phi =0.0064 at 532 nm. Continuous photolysis studies reveal that the quantum yield for the net photodecomposition o f 1 is much smaller (10(-4)). Thus, (MnTPP)-T-II produced by laser pho tolysis of (MnTPP)-T-III(ONO) mostly returns to 1 by recombination wit h NO2 according to second-order kinetics with a rate constant 2.2 x 10 (9) M-1 s(-1). The kinetics for the reactions of (MnTPP)-T-II with O-2 , NO, and pyridine were investigated in detail. In aerated toluene, (M nTPP)-T-II reversibly reacts with oxygen to yield the dioxygen adduct, MnTPP(O-2) (3). The rate constants, k(f)(O-2) and k(b)(O-2), for the formation and dissociation of 3 at 300 K were determined to be 1.93 x 10(7) M-1 s(-1) and 9.0 x 10(4) s(-1), respectively, and the equilibri um constant, k(f)(O-2)/k(b)(O-2), is therefore 2.1 x 10(2) M-1. (MnTPP )-T-II reacts with pyridine to give (MnTPP)-T-II(Py) with a rate const ant of 9.5 x 10(8) M-1 s(-1). (MnTPP)-T-II reacts with NO to yield nit rosylmanganese porphyrin, (MnTPP)-T-II(NO), with the rate constant 5.3 x 10(8) M-1 s(-1). The association reactions of (MnTPP)-T-II with NO, pyridine, O-2, and NO2 are discussed in comparison with those of othe r metalloporphyrins.