Frontispiece: 10‐Silacorroles Exhibiting Near‐Infrared Absorption and Emission
Jump to 1000 nm! In this picture, the effect of heteroatoms in 10‐heterocorroles, heteroatom‐containing porphyrin analogs, on their absorption wavelengths is illustrated. As compared to several other elements incorporated into the 10‐heterocorrole skeleton, silicon is powerful enough to push the abs...
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Veröffentlicht in: | Chemistry : a European journal 2017-06, Vol.23 (33), p.n/a |
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creator | Omori, Hiroto Hiroto, Satoru Shinokubo, Hiroshi |
description | Jump to 1000 nm! In this picture, the effect of heteroatoms in 10‐heterocorroles, heteroatom‐containing porphyrin analogs, on their absorption wavelengths is illustrated. As compared to several other elements incorporated into the 10‐heterocorrole skeleton, silicon is powerful enough to push the absorption band into the near‐infrared (NIR) region through σ*–π* conjugation. NIR absorption and emission dyes are promising materials for applications in bioimaging, photodynamic therapy, and solar energy conversion. For more information, see the Communication by H. Omori, S. Hiroto, and H. Shinokubo on page 7866 ff. |
doi_str_mv | 10.1002/chem.201783363 |
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In this picture, the effect of heteroatoms in 10‐heterocorroles, heteroatom‐containing porphyrin analogs, on their absorption wavelengths is illustrated. As compared to several other elements incorporated into the 10‐heterocorrole skeleton, silicon is powerful enough to push the absorption band into the near‐infrared (NIR) region through σ*–π* conjugation. NIR absorption and emission dyes are promising materials for applications in bioimaging, photodynamic therapy, and solar energy conversion. For more information, see the Communication by H. Omori, S. Hiroto, and H. 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In this picture, the effect of heteroatoms in 10‐heterocorroles, heteroatom‐containing porphyrin analogs, on their absorption wavelengths is illustrated. As compared to several other elements incorporated into the 10‐heterocorrole skeleton, silicon is powerful enough to push the absorption band into the near‐infrared (NIR) region through σ*–π* conjugation. NIR absorption and emission dyes are promising materials for applications in bioimaging, photodynamic therapy, and solar energy conversion. For more information, see the Communication by H. Omori, S. Hiroto, and H. 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In this picture, the effect of heteroatoms in 10‐heterocorroles, heteroatom‐containing porphyrin analogs, on their absorption wavelengths is illustrated. As compared to several other elements incorporated into the 10‐heterocorrole skeleton, silicon is powerful enough to push the absorption band into the near‐infrared (NIR) region through σ*–π* conjugation. NIR absorption and emission dyes are promising materials for applications in bioimaging, photodynamic therapy, and solar energy conversion. For more information, see the Communication by H. Omori, S. Hiroto, and H. Shinokubo on page 7866 ff.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/chem.201783363</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5321-2205</orcidid><orcidid>https://orcid.org/0000-0002-5363-4758</orcidid></addata></record> |
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subjects | 10-heterocorroles Absorption Absorption spectra Analogs Chemistry Conjugation Direct power generation Dyes dyes/pigments Emission Energy Energy conversion I.R. radiation Infrared absorption Medical imaging Near infrared radiation NIR emission Photodynamic therapy porphyrinoids Silicon Solar energy Solar energy conversion Wavelengths |
title | Frontispiece: 10‐Silacorroles Exhibiting Near‐Infrared Absorption and Emission |
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