Jonathon Tanks
(National Institute for Materials Science
)
;
Takashi Hiroi
(National Institute for Materials Science
)
;
Kenji Tamura
(National Institute for Materials Science
)
;
Kimiyoshi Naito
(National Institute for Materials Science
)
説明:
(abstract)The dynamic covalent chemistry of molecular disulfides has been studied extensively in solution, but their reactivity when confined to nanospaces has not been investigated, nor has their application to functional nanomaterials been explored. In this study, symmetrical organic disulfides were tethered to the basal planes of synthetic mica by intercalation, confining photo-induced reactions to the interlayer as a result. This approach functionalizes the nanosheets to act as host for photo-induced disulfide-disulfide, disulfide-thiol, and disulfide-ene reactions, providing control and versatility for a wide variety of applications.
権利情報:
©2022 The Chemical Society of Japan
キーワード: Disulfide chemistry, Layered silicates, Photo-reactivity
刊行年月日: 2023-01-15
出版者: The Chemical Society of Japan
掲載誌:
研究助成金:
原稿種別: 著者最終稿 (Accepted manuscript)
MDR DOI: https://doi.org/10.48505/nims.4302
公開URL: https://doi.org/10.1246/bcsj.20220309
関連資料:
その他の識別子:
連絡先:
更新時刻: 2024-01-05 22:12:44 +0900
MDRでの公開時刻: 2023-12-12 13:30:27 +0900
| ファイル名 | サイズ | |||
|---|---|---|---|---|
| ファイル名 |
Tethering Organic Disulfides_proof.pdf
application/pdf |
サイズ | 449KB | 詳細 |
| ファイル名 |
Tethering Organic Disulfides_ESI.pdf
(サムネイル)
application/pdf |
サイズ | 4.51MB | 詳細 |