Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Younis Ahmad, Pandit"'
Publikováno v:
Dalton Transactions. 52:877-891
A dinickel(II)porphyrin dimer has been used here in which the redox-active pyrrole-moiety, similar to the tryptophan residue in diheme enzymes such as MauG and bCcP, has been placed between two Ni(II)porphyrin centers connected
Autor:
Younis Ahmad Pandit, Syed Jehanger Shah, Mohammad Usman, Sabyasachi Sarkar, Eugenio Garribba, Sankar Prasad Rath
Publikováno v:
Inorganic chemistry. 61(13)
Dinickel(II) and dicopper(II) porphyrin dimers have been constructed in which two metalloporphyrin units are widely separated by a long unconjugated dipyrrole bridge. Two macrocycles are aligned somewhat orthogonally to each other, while oxidation of
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 644:856-863
Publikováno v:
Chemistry - A European Journal. 23:13415-13422
This work reports a highly facile one-pot synthesis of a new series of fully π-conjugated unsymmetric chlorin-porphyrin heterodimers with quantitative yields by utilizing intermacrocyclic interactions. One-electron oxidations of dicopper(II) and dip
Publikováno v:
Chemistry – A European Journal. 23:10270-10275
MauG is a diheme enzyme that utilizes two covalently bound c-type heme centers. We report here step-wise oxidations of a synthetic analogue of MauG in which two heme centers are bridged covalently through a flexible linker containing a pyrrole moiety
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 23(43)
MauG is a diheme enzyme that utilizes two covalently bound c-type heme centers. We report here step-wise oxidations of a synthetic analogue of MauG in which two heme centers are bridged covalently through a flexible linker containing a pyrrole moiety
Publikováno v:
Inorganic chemistry. 55(7)
The interaction between two porphyrin macrocycles, connected covalently through either a rigid ethylene or a flexible ethane bridge, in the metalloporphyrin dimers (M: 2H, Zn(2+)) have been investigated upon stepwise oxidations. Upon 1e-oxidation, tw