Marked difference in singlet-chemiexcitation efficiency between syn-anti isomers of spiro[1,2-dioxetane-3,1′-dihydroisobenzofuran] for intramolecular charge-transfer-induced decomposition

Tetrahedron Letters

Volumn 49, Issue 42, 2008, Pages 6145-6147

  Matsumoto, Masakatsu ^a   Takamido, Yuka ^a   Nomura, Kana ^a   Shiono, Tamaki ^a   Watanabe, Nobuko ^a   Ijuin, Hisako K ^a  

^a KANAGAWA UNIVERSITY   (Japan)

Author keywords

Chemiluminescence; Dioxetane; Singlet chemiexcitation

Indexed keywords

DIMETHYL SULFOXIDE; FURAN DERIVATIVE; HYDROXYL GROUP; SPIRO[1,2 DIOXETANE 3,1' DIHYDROISOBENZOFURAN]; TETRABUTYLAMMONIUM; TETRABUTYLAMMONIUM FLUORIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHEMOLUMINESCENCE; CRYSTAL STRUCTURE; DECOMPOSITION; INFRARED SPECTROSCOPY; ISOMERISM; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 50549103105     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.024     Document Type: Article

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13. 4: C, 73.15; H, 7.37. Found: C, 72.78; H, 7.69.
14. -3. CCDC deposition number: 690663.These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Center, 12 Union Road, Cambridge CB21EZ, UK; fax: (+44)1223 336 033; or e-mail: deposit@ccdc.cam.au.uk).
15. CL = 0.29). 11
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