Reaction mechanisms relevant to the formation of iron and ruthenium nitric oxide complexes

被引:81
作者
Ford, PC [1 ]
Laverman, LE [1 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
基金
美国国家科学基金会;
关键词
nitric oxide; reaction mechanisms; ruthenium; iron; kinetics;
D O I
10.1016/j.ccr.2004.04.006
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Presented here is a review of recent mechanistic work related to the formation of iron and ruthenium nitrosyl complexes. Given the importance of NO as a biological molecule and that the targets for NO in vivo are metal centers, knowledge of the mechanisms by which metal nitrosyls are formed is fundamental for understanding the diverse roles that NO plays in biology. The kinetics of metal nitrosyl formation from the reactions of free NO with metal complex precursors are dominated by the lability of the complexes. The free radical character of NO however, asserts itself especially if the precursors are relatively substitution inert or are coordinatively unsaturated. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:391 / 403
页数:13
相关论文
共 111 条
[1]   Nitric oxide is a physiological substrate for mammalian peroxidases [J].
Abu-Soud, HM ;
Hazen, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37524-37532
[2]   Peroxidases inhibit nitric oxide (NO) dependent bronchodilation: Development of a model describing NO-peroxidase interactions [J].
Abu-Soud, HM ;
Khassawneh, MY ;
Sohn, JT ;
Murray, P ;
Haxhiu, MA ;
Hazen, SL .
BIOCHEMISTRY, 2001, 40 (39) :11866-11875
[3]   Electron transfer, oxygen binding, and nitric oxide feedback inhibition in endothelial nitric-oxide synthase [J].
Abu-Soud, HM ;
Ichimori, K ;
Presta, A ;
Stuehr, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17349-17357
[4]   Kinetics and equilibria in ligand binding by nitrophorins 1-4: Evidence for stabilization of a nitric oxide-ferriheme complex through a ligand-induced conformational trap [J].
Andersen, JF ;
Ding, XD ;
Balfour, C ;
Shokhireva, TK ;
Champagne, DE ;
Walker, FA ;
Montfort, WR .
BIOCHEMISTRY, 2000, 39 (33) :10118-10131
[5]   Kinetics studies of the reaction of the ruthenium porphyrin Ru(OEP)(CO) with the S-nitrosothiol N-acetyl-1-amino-2-methylpropyl-2-thionitrite [J].
Andreasen, LV ;
Lorkovic, IM ;
Richter-Addo, GB ;
Ford, PC .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2002, 6 (02) :228-235
[6]   A BIMOLECULAR MECHANISM FOR SUBSTITUTION [J].
ARMOR, JN ;
SCHEIDEGGER, HA ;
TAUBE, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (21) :5928-+
[7]   INFLUENCE OF PH AND IONIC-STRENGTH UPON SOLUBILITY OF NO IN AQUEOUS-SOLUTION [J].
ARMOR, JN .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1974, 19 (01) :82-84
[8]   Fast nitroxyl trapping by ferric porphyrins [J].
Bari, SE ;
Martí, MA ;
Amorebieta, VT ;
Estrin, DA ;
Doctorovich, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (50) :15272-15273
[9]   ELECTROCATALYTIC REDUCTION OF NITRITE TO AMMONIA BASED ON A WATER-SOLUBLE IRON PORPHYRIN [J].
BARLEY, MH ;
TAKEUCHI, KJ ;
MEYER, TJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (19) :5876-5885
[10]   Synthesis and axial ligand substitution chemistry of Ru(TTP)(NO)X. Structures of Ru(TTP)(NO)X (X = ONO, OH) [J].
Bohle, DS ;
Hung, CH ;
Smith, BD .
INORGANIC CHEMISTRY, 1998, 37 (22) :5798-5806