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  1. 研究論文

The photochemical reactions of nitrogen-rich mesoionic 1,3-diphenyltetrazolium heterocycles and related compounds

https://nitech.repo.nii.ac.jp/records/4997
https://nitech.repo.nii.ac.jp/records/4997
35fad465-a45e-48b4-8c3c-fa9a87d919c5
名前 / ファイル ライセンス アクション
JCSP 本文_fulltext (146.7 kB)
J. CHEM. SOC. PERKIN TRANS. I 2001, 2476-2482 - Reproduced by permission of The Royal Society of Chemistry (RSC)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2012-11-06
タイトル
タイトル The photochemical reactions of nitrogen-rich mesoionic 1,3-diphenyltetrazolium heterocycles and related compounds
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Araki, Shuki

× Araki, Shuki

en Araki, Shuki

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Hattori, Hiromi

× Hattori, Hiromi

en Hattori, Hiromi

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Ogawa, Koji

× Ogawa, Koji

en Ogawa, Koji

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Kuzuya, Masashi

× Kuzuya, Masashi

en Kuzuya, Masashi

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Inoue, Tomoko

× Inoue, Tomoko

en Inoue, Tomoko

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Yamamura, Hatsuo

× Yamamura, Hatsuo

en Yamamura, Hatsuo

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Kawai, Masao

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en Kawai, Masao

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著者別名
姓名 荒木, 修喜
著者別名
姓名 山村, 初雄
書誌情報 en : Journal of the Chemical Society. Perkin transactions 1

巻 2001, 号 19, p. 2476-2482, 発行日 2001-09-11
出版者
出版者 Royal Society of Chemistry
言語 en
ISSN
収録物識別子タイプ ISSN
収録物識別子 1472-7781
item_10001_source_id_32
収録物識別子タイプ NCID
収録物識別子 AA11413675
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
item_10001_relation_34
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 http://dx.doi.org/10.1039/B009526P
関連名称 10.1039/B009526P
内容記述
内容記述タイプ Other
内容記述 Photochemical reactions of azo and triazo derivatives of mesoionic 1,3-diphenyltetrazolium heterocycles and related compounds were studied. The reaction paths were found to depend markedly on the types of substrate, substituent and reaction solvent giving diverse products. Upon irradiation of the 1,1′3,3′-tetraphenylazoditetrazolium salt 1, the addition of hydrogen and acetone to the NN bond was observed in methanol and acetone, respectively, whereas the bond was cleaved in diethyl ketone to give the 5-aminotetrazolium salt 10. The corresponding radical cation 11 also gave the reduction product in methanol. On the other hand, the 1,3-diphenyl-5-(phenylazo)tetrazolium salt 12 underwent nitrogen evolution giving the 1,3-diphenyltetrazolium salt 13via the corresponding tetrazolium radical. Triazene derivatives 14 and 17 underwent an N-N bond cleavage to give tetrazolio-5-amide 4. The mesoionic triazene compounds bearing a tosyl 18 or cyano group 19 gave products 20 and 23. Triphenylphosphinotriazene 24 liberated nitrogen to give phosphinoimide 25 and its hydrolysis product 10. Tetrazolylamide 26 lost a phenyldiazonium group from the 1,3-diphenyltetrazolium ring to give the guanidine derivative 27.
言語 en
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