TY - JOUR
T1 - Sterically hindered benzoates
T2 - A synthetic strategy for modeling dioxygen activation at diiron active sites in proteins
AU - Tolman, William B.
AU - Que, Lawrence
PY - 2002
Y1 - 2002
N2 - Bulky terphenyl carboxylates and related benzylsubstituted benzoates have been used to assemble a variety of new diiron complexes analogous to nonheme diiron protein active sites. Through this conceptually simple approach, novel biomimetic structures have been accessed and biologically relevant oxidized intermediates and products have been isolated and characterized by both spectroscopic and X-ray crystallographic methods. Interesting similarities and differences in the observed chemistry of the iron(n) complexes, including ligand substitution and dioxygen activation reactions, result from variation of the specific carboxylate and accompanying N-donor ligand structures. As a result, new insights have been obtained into structure/function relationships in carboxylate-rich nonheme diiron proteins.
AB - Bulky terphenyl carboxylates and related benzylsubstituted benzoates have been used to assemble a variety of new diiron complexes analogous to nonheme diiron protein active sites. Through this conceptually simple approach, novel biomimetic structures have been accessed and biologically relevant oxidized intermediates and products have been isolated and characterized by both spectroscopic and X-ray crystallographic methods. Interesting similarities and differences in the observed chemistry of the iron(n) complexes, including ligand substitution and dioxygen activation reactions, result from variation of the specific carboxylate and accompanying N-donor ligand structures. As a result, new insights have been obtained into structure/function relationships in carboxylate-rich nonheme diiron proteins.
UR - http://www.scopus.com/inward/record.url?scp=0036026570&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0036026570&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0036026570
SN - 1470-479X
SP - 653
EP - 660
JO - Journal of the Chemical Society, Dalton Transactions
JF - Journal of the Chemical Society, Dalton Transactions
IS - 5
ER -