Journal
ORGANOMETALLICS
Volume 31, Issue 19, Pages 6834-6842Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om300642b
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Funding
- Japan Society for Promotion of Science [22750108]
- Ministry of Education, Culture, Sports, Science and Technology of Japan
- Ogasawara Foundation for the Promotion of Science Engineering
- Sumitomo Foundation
- Grants-in-Aid for Scientific Research [22750108] Funding Source: KAKEN
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The structures of [(2,5-norbornadiene)Rh{C-(Ph)=CPh2)(PPh3)] (1) and its reaction product with CH3CO2H were elucidated by H-1, C-13, and P-31 NMR spectroscopy, mass spectrometry, and single-crystal X-ray analysis. The presence of two conformational isomers of 1 was verified by NMR spectroscopy, which was well-supported by DFT calculations. Phenylacetylene was polymerized using 1 as a catalyst with [M](0)/[Rh] = 10 and quenched with CH3CO2H and CH3CO2D. The incorporation of H and D at the polymer ends was confirmed by MALDI-TOF mass spectrometry and H-1 and H-1-C-13 HSQC NMR spectroscopy. The polymerization degree was calculated to be 11 by H-1 NMR spectroscopy, which agreed well with the theoretical value.
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