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Quantum mechanical study of the oxidation pathway of the oxygen‐evolving catalyst, [(bpy) 2 (H 2 O)Ru III –O–Ru III (H 2 O)(bpy) 2 ] +4 *
Author(s) -
Bartolotti L. J.,
Pedersen L. G.,
Meyer T. J.
Publication year - 2001
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.1206
Subject(s) - catalysis , chemistry , density functional theory , crystallography , bipyridine , oxygen atom , ruthenium , water splitting , molecule , computational chemistry , photocatalysis , crystal structure , organic chemistry
Quantum mechanical density functional calculations are performed for the various oxidized forms of the water‐oxidation catalyst [(bpy) 2 (H 2 O)Ru III – O–Ru III (H 2 O)(bpy) 2 ] +4 (where bpy is 2,2′‐bipyridine). Two possible structural forms of [(bpy) 2 (H 2 O)Ru–O–Ru(H 2 O)(bpy) 2 ] +4 are investigated. One has two of the interior to two waters bpy ligands and the other has the two water ligands exterior. Our calculations show the interior form to be around 4 kcal/mol lower in energy. The calculated electronic structures for the interior form [(bpy) 2 (H 2 O)Ru–O–Ru(H 2 O)(bpy) 2 ] +4 and the exterior from [(bpy) 2 (H 2 O)Ru–O–Ru(OH)(bpy) 2 ] +4 compare well with structures determined from X‐ray crystallography. © 2001 John Wiley & Sons, Inc. Int J Quant Chem 83: 143–149, 2001