期刊
ORGANOMETALLICS
卷 30, 期 21, 页码 6034-6043出版社
AMER CHEMICAL SOC
DOI: 10.1021/om200913c
关键词
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资金
- UF
- Alfred P. Sloan Foundation
- Camille and Henry Dreyfus Foundation
- NSF [CHE-0821346]
A series of eight [(diNHC)Rh(CO)(2)][OTf] complexes, 1'-R, 2'-R, and 3'-R (where diNHC = DEAM, trans-9,10-dihydro-9,10-ethancianthracene-11,12-diylmethane-diyl carbene, and DEA, trans-9,10-dihydro-9,10-ethanopthracene-11,12-diyl carbene ligands; R = R-methylphenylmethane (R-CHMePh), diphenylmethane (diPh), benzyl (Bn), methyl (Me), isopropyl (Pr-t), and o-methylbenzyl (o-MeBn); carbene heterocycle = imidazol-2-ylidene, and benzimidazol-2-ylidene), are synthesized and characterized. The purpose for the synthesis of these complexes was to examine the relationship between carbene N-heterocycle, R-group substitution, and metallocycle ring size (DEAM = 9, DEA = 7 atom ring) on ligand flexibility. The complexes were examined by chemical exchange saturation transfer to measure the rate of conformational isomerization. The results indicate that flexibility is not significantly altered by choice of carbene heterocycle and R group. However, the constrained DEA diNHC derivative does not undergo conformational isomerization.
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