The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
meso, meso‐Linked Porphyrin Arrays
Abstract
The perpendicular arrangement of porphyrin units in dimer 1 is reflected in a large excitonic coupling that leads to splitting of the Soret bands and only modest spectral changes in the Q-bands. Compound 1 and the analogous trimer and tetramer are prepared by oxidative coupling of the corresponding 5,15-diarylporphyrin and are the first examples of compounds having direct meso, meso-linked porphyrin chromophores. Ar = 3,5-tBu2C6H3.
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Cites
Photoinduced electron transfer in supramolecular systems for artificial photosynthesis
Wasielewski, M. R. (1992) · Chemical Reviews · doi:10.1021/cr00011a005 · Cited by 3,083
Energy Transfer Mechanisms and the Molecular Exciton Model for Molecular Aggregates
Kasha, M. (1963) · Radiation Research · doi:10.2307/3571331 · Cited by 1,652
Highly Conjugated, Acetylenyl Bridged Porphyrins: New Models for Light-Harvesting Antenna Systems
Lin, V. S.-Y., DiMagno, S. G., & Therien, M. J. (1994) · Science · doi:10.1126/science.8178169 · Cited by 694
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Wagner, R. W., & Lindsey, J. S. (1994) · Journal of the American Chemical Society · doi:10.1021/ja00100a055 · Cited by 473
.pi.-Cation radicals and dications of metalloporphyrins
Fajer, J., Borg, D. C., Forman, A., Dolphin, D., & Felton, R. H. (1970) · Journal of the American Chemical Society · doi:10.1021/ja00714a038 · Cited by 458
Wagner, R. W., Johnson, T. E., Li, F., & Lindsey, J. S. (1995) · The Journal of Organic Chemistry · doi:10.1021/jo00121a052 · Cited by 305
Synthesis of naphthalene-bridged porphyrin dimers and their orientation-dependent exciton coupling
Osuka, A., & Maruyama, K. (1988) · Journal of the American Chemical Society · doi:10.1021/ja00221a079 · Cited by 276
Self-citationBuilding-block synthesis of porphyrin light-harvesting arrays
Prathapan, S., Johnson, T. E., & Lindsey, J. S. (1993) · Journal of the American Chemical Society · doi:10.1021/ja00069a068 · Cited by 273
Synthesis and Third‐Order Nonlinear Optical Properties of a Conjugated Porphyrin Polymer
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Cited by
Conjugated porphyrin arrays: synthesis, properties and applications for functional materials
Tanaka, T., & Osuka, A. (2015) · Chemical Society Reviews · doi:10.1039/c3cs60443h · Cited by 699
Self-citationSynthetic Routes to Multiporphyrin Arrays
Burrell, A. K., Officer, D. L., Plieger, P. G., & Reid, D. C. W. (2001) · Chemical Reviews · doi:10.1021/cr0000426 · Cited by 414
Giant Multiporphyrin Arrays as Artificial Light-Harvesting Antennas
Imahori, H. (2004) · The Journal of Physical Chemistry B · doi:10.1021/jp038036b · Cited by 353
Multiporphyrinic Cages: Architectures and Functions
Durot, S., Taesch, J., & Heitz, V. (2014) · Chemical Reviews · doi:10.1021/cr400673y · Cited by 295
Umeyama, T., Takamatsu, T., Tezuka, N., Matano, Y., Araki, Y., Wada, T., Yoshikawa, O., Sagawa, T., Yoshikawa, S., & Imahori, H. (2009) · The Journal of Physical Chemistry C · doi:10.1021/jp902001z · Cited by 119
Metadata
- Authors
- Osuka, A., & Shimidzu, H.
- Venue
- Angewandte Chemie International Edition in English
- Publisher
- Wiley
- Published
- 1997-02-03
- Volume
- 36
- Issue
- 1-2
- Pages
- 135-137
- ISSN
- 0570-0833 (ISSN-L)
- OpenAlex
- W2162540376
- Cited by
- 434
- References
- 14
- FWCI
- 16.67
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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