Photoinduced carbon monoxide migration in a synthetic heme-copper complex

Journal of the American Chemical Society

Volumn 127, Issue 17, 2005, Pages 6225-6230

  Fry, H Christopher ^a   Cohen, Andrew D ^a   Toscano, John P ^a   Meyer, Gerald J ^a   Karlin, Kenneth D ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION; COPPER COMPOUNDS; MOLECULES; ULTRAVIOLET SPECTROSCOPY;

CARBON MONOXIDE MIGRATION; COPPER COMPLEX; DIRECT TRANSFER; HEME-COPPER COMPOUND;

CARBON MONOXIDE;

ACETONE; CARBON MONOXIDE; COPPER; CYTOCHROME C OXIDASE; HEME;

ABSORPTION; ARTICLE; CHEMICAL REACTION KINETICS; DISSOCIATION; PHOTOLYSIS; ROOM TEMPERATURE; SPECTROSCOPY; SYNTHESIS; TEMPERATURE DEPENDENCE; ULTRAVIOLET RADIATION;

CARBON MONOXIDE; COPPER; HEME; IRON COMPOUNDS; KINETICS; MODELS, MOLECULAR; PHOTOLYSIS; SPECTROPHOTOMETRY, INFRARED; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 18244406816     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja043199e     Document Type: Article

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62. 2) measured by TA and TRIR could be attributed to increased sample concentrations and lack of full temperature control.
63. + because the spectra of these two complexes (from 350 to 600 nm) are within experimental error of one another (being dominated by the π-π* transitions of the heme).