Photolability of NO in designed metal nitrosyls with carboxamido-N donors: a theoretical attempt to unravel the mechanism

2012 ◽  
Vol 41 (16) ◽  
pp. 4726 ◽  
Author(s):  
Nicole L. Fry ◽  
Pradip K. Mascharak
Keyword(s):  
1962 ◽  
Vol 84 (17) ◽  
pp. 3404-3405 ◽  
Author(s):  
Harry B. Gray ◽  
Ivan. Bernal ◽  
Ernst. Billig

1985 ◽  
Vol 281 (2-3) ◽  
pp. 263-272 ◽  
Author(s):  
Peter Oltmanns ◽  
Dieter Rehder

1974 ◽  
Vol 5 (22) ◽  
pp. no-no
Author(s):  
G. INNORTA ◽  
S. TORRONI ◽  
A. FOFFANI

1999 ◽  
Vol 21 (1-3) ◽  
pp. 131-148 ◽  
Author(s):  
Dmitry V. Fomitchev ◽  
Philip Coppens

Author(s):  
GEORGE B. RICHTER-ADDO

The chemistry of nitric oxide (NO) has taken on new dimensions since the discovery, about a decade ago, of a myriad of biological events that NO participates in. Many of the foundations of metal-NO chemistry were laid out earlier by inorganic chemists and biochemists investigating the structures and electronic properties of the heme-NO moiety or its model compounds. Certainly, the persistent work over the last three decades by chemists working with metal nitrosyls has paid off. Current areas of research in heme-NO chemistry include (i) how the NO group approaches and binds to the metal center (or how it dissociates from the metal center); (ii) the ground state and excited state geometries of the metal-NOfragment; (iii) effects of the trans axial ligands on NO orientation and/or dissociation; and (iv) N-N bond formation from NO molecules catalyzed by heme groups.


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