Zobrazeno 1 - 10
of 148
pro vyhledávání: '"J. K. KOCHI"'
Publikováno v:
The Journal of Physical Chemistry. 98:3865-3871
Laser excitation of charge-transfer complexes between pyridinium-analogous acceptors and arene donors incorporated into zeolite-Y and zeolite-L generates transient radical ion pairs that can be monitored using time-resolved diffuse-reflectance spectr
Autor:
S. Sankararaman, J. K. Kochi
Publikováno v:
ChemInform. 22
The transient intermediates accompanying the charge-transfer excitation of the 1,4-dimethylnaphthalene (DMN) complex with either the N-nitropyridinium or tetranitromethane acceptor are identified as the cation radical DMN+˙ paired with NO2 and eithe
Publikováno v:
ChemInform. 24
Autor:
T. M. BOCKMAN, J. K. KOCHI
Publikováno v:
ChemInform. 25
Autor:
J. K. Kochi, R. Rathore
Publikováno v:
ChemInform. 27
Publikováno v:
Inorganic Chemistry. 31:3943-3950
Ligand-field spectra and infrared spectra of compounds with stoichiometry M(LLL)X, where X is one of the pseudohalides NCS - , NCO, and N 3 - , LLL - is a tridentate-substituted pyrazolylborate monoanionic ligand, and M=Ni (as well as a number of Co
Autor:
Z. J. Karpinski, J. K. Kochi
Publikováno v:
Inorganic Chemistry. 31:2762-2767
Electron-transfer chain (ETC) catalysis in the facile electroreductive deligation or a series or bis(arene)iron(II) dications is established by the application or normal pulse (NP) and reverse pulse (RP) voltammetry in acetonitrile solution
Autor:
J. K. Kochi, T. Yabe
Publikováno v:
Journal of the American Chemical Society. 114:4491-4500
Direct observation by time-resolved picosecond spectroscopy of the contact ion pair (CIP) allows the microdynamical rate constants for its (a) annihilation by internal return, (b) relaxation to the solvent-separated ion pair (SSIP), and (c) ionic exc
Autor:
S. Wolowiec, J. K. Kochi
Publikováno v:
Inorganic Chemistry. 30:1215-1221
The oxidative decarbonylation of the tricarbonylrhenium(I) and -molybdenum(0) complexes Cp*Re(CO) 3 (I, Cp*=pentamethylcyclopentadienide) and TpMo(CO) 3 − (II, Tp=hydridotris(1-pyrazolyl) borate) occurs quantitatively to the corresponding trioxo co
Autor:
Tadashi Mori, S. V. Lindeman, C.-J. Zhu, J. K. Kochi, Rajendra Rathore, Paul von Ragué Schleyer
Publikováno v:
The Journal of organic chemistry. 67(15)
Access to each C=C face of adamantylideneadamantane (AA) and sesquihomoadamantene (SA) is hindered by the hydrogenic canopy consisting of four beta-hydrogens; otherwise, these olefins have quite normal environments. X-ray crystallography and density