抄録
10-Silacorroles were obtained from the Pd-catalyzed silylative cyclization of a bis(α,α′-dibromodipyrrin) Ni^II precursor with dihydrosilanes. These 10-silacorroles show substantially red-shifted absorption bands relative to those of normal porphyrins and isocorroles. Notably, the corresponding free base and Zn^II 10-silacorroles exhibit emissions in the NIR region. Theoretical calculations on these 10-silacorroles revealed the presence of σ*–π* conjugation between the silyl group and the tetrapyrrole π system, which significantly lowers their LUMO energy levels.
収録刊行物
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- CHEMISTRY-A EUROPEAN JOURNAL
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CHEMISTRY-A EUROPEAN JOURNAL 22 (33), 7866-7870, 2017-06-12
Wiley
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詳細情報 詳細情報について
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- CRID
- 1050564288759295360
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- NII論文ID
- 120006349126
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- HANDLE
- 2237/26985
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- ISSN
- 09476539
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- CiNii Articles
- KAKEN