DIOXYGEN-INDUCED DECARBOXYLATION AND HYDROXYLATION OF [NI-II(GLYCYL-GLYCYL-L-HISTIDINE)] OCCURS VIA NI-III - X-RAY CRYSTAL-STRUCTURE OF [NI-II(GLYCYL-GLYCYL-ALPHA-HYDROXY-D,L-HISTAMINE)]CENTER-DOT-3H2O

被引:91
作者
BAL, W
DJURAN, MI
MARGERUM, DW
GRAY, ET
MAZID, MA
TOM, RT
NIEBOER, E
SADLER, PJ
机构
[1] UNIV LONDON BIRKBECK COLL,DEPT CHEM,GORDON HOUSE & CHRISTOPHER INGOLD LABS,LONDON WC1H 0PP,ENGLAND
[2] PURDUE UNIV,DEPT CHEM,W LAFAYETTE,IN 47907
[3] UNIV WALES COLL CARDIFF,SCH CHEM & APPL CHEM,CARDIFF CF1 3TB,WALES
[4] MCMASTER UNIV,HLTH SCI CTR,DEPT BIOCHEM,HAMILTON L8N 3Z5,ON,CANADA
关键词
D O I
10.1039/c39940001889
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical and EPR studies show that the dioxygen-induced decarboxylation and hydroxylation of [Ni-II(GGH-H--2)](-), where GGH is glycyl-glycyl-L-histidine (HL), in aqueous solution occurs via a Ni-III intermediate; the product [Ni-II(Gly-Gly-alpha-hydroxy-D,L-histamine-H-2)].3H(2)O is shown by X-ray crystallography to contain square-planar Ni-II coordinated to the terminal amino group [Ni-N, 1:932(3) Angstrom], two deprotonated amide N's [1.884(3) and 1.831(3) Angstrom] and imidazole delta N [1.908(3) Angstrom].
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页码:1889 / 1890
页数:2
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