Abstract
Abstract Diastereomerically pure 2,5-piperazinedione-bridged meso-tetraarylporphyrin dimers were synthesized with easy procedures. 1H NMR, UV-vis, and CD spectra showed that porphyrin moieties in the l,l-molecule interacted more strongly than those in the d,l-isomer and this interaction decreased with substitution by 3,5-di-t-butyl groups on the meso-phenyl substituents.
References
14
Referenced
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Dates
Type | When |
---|---|
Created | 19 years ago (Aug. 11, 2006, 1:35 a.m.) |
Deposited | 1 year, 7 months ago (Jan. 19, 2024, 5:16 p.m.) |
Indexed | 1 year ago (July 30, 2024, 6:33 a.m.) |
Issued | 31 years, 11 months ago (Sept. 1, 1993) |
Published | 31 years, 11 months ago (Sept. 1, 1993) |
Published Online | 19 years ago (Aug. 11, 2006) |
Published Print | 31 years, 11 months ago (Sept. 1, 1993) |
@article{Tamiaki_1993, title={Intramolecular Interaction of Porphyrin Moieties in 2,5-Piperazinedione-Bridged Porphyrin Dimers}, volume={66}, ISSN={1348-0634}, url={http://dx.doi.org/10.1246/bcsj.66.2633}, DOI={10.1246/bcsj.66.2633}, number={9}, journal={Bulletin of the Chemical Society of Japan}, publisher={Oxford University Press (OUP)}, author={Tamiaki, Hitoshi and Suzuki, Shinji and Maruyama, Kazuhiro}, year={1993}, month=sep, pages={2633–2637} }