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Volumn 7, Issue 23, 2001, Pages 5070-5083

S-position isomers of BEDT-TTF and EDT-TTF: Synthesis and influence of outer sulfur atoms on the electrochemical properties and crystallographic network of related organic metals

Author keywords

BEDT TTF isomers; Crystal engineering; Organic materials; Sulfur heterocycles; Tetrathiafulvalene

Indexed keywords

CRYSTALLOGRAPHY; ELECTROCHEMISTRY; ELECTRONIC PROPERTIES; POSITIVE IONS; SALTS; SULFUR; ULTRAVIOLET SPECTROSCOPY;

EID: 85047700452     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (62)

References (96)
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    • We later succeeded in synthesizing the powerful 2,3-bis(bromomethyl)TTF derivatives, which could be transformed into the corresponding thiolesters upon treatment with potassium thioacetate: P. Hudhomme, S. G. Liu, D. Kreher, M. Cariou, A. Gorgues, Tetrahedron Lett. 1999, 40, 2927-2930.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2927-2930
    • Hudhomme, P.1    Liu, S.G.2    Kreher, D.3    Cariou, M.4    Gorgues, A.5
  • 42
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    • b) D. L. Hughes in Organic Reactions, Wiley, New York, 1992, 42, 335-656.
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    • Hughes, D.L.1
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    • The oxidation of thiol compounds into the corresponding disulfides has previously been reported to be achievable by use of molecular oxygen as oxidant in the presence of strong bases, aliphatic amines, metal ions, aluminium oxide, or silica gel as catalysts: K.-T. Liu, Y.-C. Tong, Synthesis, 1978, 669-670, and references therein.
    • (1978) Synthesis , pp. 669-670
    • Liu, K.-T.1    Tong, Y.-C.2
  • 60
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    • This reaction was previously presented in a Poster Communication: "Journée de la Société Française de Chimie", Piriac-France, 30-31 May 1996
    • This reaction was previously presented in a Poster Communication: "Journée de la Société Française de Chimie", Piriac-France, 30-31 May 1996.
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    • 3 has been observed for thionolactone to afford the corresponding lactone: S. Ayral-Kaloustian, W. C. Agosta, Synth. Commun. 1981, 11, 1011-1015.
    • (1981) Synth. Commun. , vol.11 , pp. 1011-1015
    • Ayral-Kaloustian, S.1    Agosta, W.C.2
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    • Triethylphosphite is known to react with diethyl disulfide to yield diethyl-sulfide and the corresponding ethylthiodiethylphosphonate. See p. 621 (loc. cit.) and A. Schönberg, M. Z. Barakat, J. Chem. Soc. 1949, 892.
    • (1949) J. Chem. Soc. , vol.892
    • Schönberg, A.1    Barakat, M.Z.2
  • 80
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    • note
    • Nevertheless, the importance of the electron-withdrawing character could not be clearly demonstrated because the first apparent oxidation potential of EDT-TTF appeared to be more positive than that corresponding to its S-position isomer 3.
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    • S. Le Moustarder, Doctoral Thesis, Université d'Angers (France) 1998.
    • (1998)
    • Le Moustarder, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.