Linked Life Data

17385851

Source:http://linkedlifedata.com/resource/pubmed/id/17385851

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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2007-4-23
pubmed:abstractText
Excitation by high-energy light, such as that of 313 nm wavelength, induces a photochemical ligand substitution (PLS) reaction of fac-[Re(bpy)(CO)3Cl] (1a) to give the solvento complexes (OC-6-34)- and (OC-6-44)-[Re(bpy)(CO)2(MeCN)Cl] (2 and 3) in good yields. The disappearance quantum yield of 1a was 0.01+/-0.001 at 313 nm. The products were isolated, and X-ray crystallographic analysis was successfully performed for 2. Time-resolved IR measurements clearly indicated that the CO ligand dissociates with subpicosecond rates after excitation, leading to vibrationally hot photoproducts, which relax within 50-100 ps. Detailed studies of the reaction mechanism show that the PLS reaction of 1a does not proceed via the lowest vibrational level in the 3MLCT excited state. The PLS reaction gives 2 and (OC-6-24)-[Re(bpy)(CO)2(MeCN)Cl] (5) as primary products, and one of the products, 5, isomerizes to 3. This type of PLS reaction is more general, occurring in various fac-rhenium(I) diimine tricarbonyl complexes such as fac-[Re(X2bpy)(CO)3Cl] (X2bpy=4,4'-X2-bpy; X=MeO, NH2, CF3), fac-[Re(bpy)(CO)3(pyridine)]+, and fac-[Re(bpy)(CO)3(MeCN)]+. The stable photoproducts (OC-6-44)- and (OC-6-43)-[Re(bpy)(CO)2(MeCN)(pyridine)]+ and (OC-6-32)- and (OC-6-33)-[Re(bpy)(CO)2(MeCN)2]+ were isolated. The PLS reaction of rhenium tricarbonyl-diimine complexes is therefore applicable as a general synthetic method for novel dicarbonyls.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0020-1669
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
46
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3531-40
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Photochemical ligand substitution reactions of fac-[Re(bpy)(CO)3Cl] and derivatives.
pubmed:affiliation
Department of Chemistry, Graduate School of Science and Engineering, Tokyo Institute of Technology, O-okayama 2-12-1, E1-9, Meguro-ku, Tokyo 152-8551, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't