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Volumn , Issue 30, 2007, Pages 4727-4735

Hybrid organic/inorganic supramolecular conductors D2[Au(CN) 4] [D = diiodo(ethylenedichalcogeno)tetrachalcogenofulvalene], including a new ambient pressure superconductor

Author keywords

Conducting materials; Iodine; Selenium heterocycles; Superconductors; Supramolecular chemistry

Indexed keywords

CRYSTAL SYMMETRY; ELECTROCHEMICAL OXIDATION; HYBRID MATERIALS; IODINE; SALTS; SELENIUM; SUPERCONDUCTING MATERIALS;

EID: 35848955407     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200700530     Document Type: Article
Times cited : (27)

References (45)
  • 17
    • 0029213661 scopus 로고
    • For other examples of organic conductors based on iodinated TTFs, see: a
    • For other examples of organic conductors based on iodinated TTFs, see: a) R. Gompper, J. Hock, K. Polborn, E. Dormann, H. Winter, Adv. Mater. 1995, 7, 41-43;
    • (1995) Adv. Mater , vol.7 , pp. 41-43
    • Gompper, R.1    Hock, J.2    Polborn, K.3    Dormann, E.4    Winter, H.5
  • 24
    • 10244264738 scopus 로고    scopus 로고
    • For reviews of organic conductors based on halogenated TTFs, see: a
    • For reviews of organic conductors based on halogenated TTFs, see: a) M. Fourmigué, P. Batail, Chem. Rev. 2004, 104, 5379-5418;
    • (2004) Chem. Rev , vol.104 , pp. 5379-5418
    • Fourmigué, M.1    Batail, P.2
  • 25
    • 85163236477 scopus 로고    scopus 로고
    • T. Imakubo in TTF Chemistry - Fundamentals and Applications of Tetrathiafulvalene: Halogenated TTFs (Eds.: J. Yamada, T. Sugimoto), Kodansha & Springer, Tokyo, 2004, chapter 3 and references cited therein.
    • b) T. Imakubo in TTF Chemistry - Fundamentals and Applications of Tetrathiafulvalene: Halogenated TTFs (Eds.: J. Yamada, T. Sugimoto), Kodansha & Springer, Tokyo, 2004, chapter 3 and references cited therein.
  • 26
    • 27144519240 scopus 로고    scopus 로고
    • For reviews of organic conductors based on selenium analogues of TTFs, see: a
    • For reviews of organic conductors based on selenium analogues of TTFs, see: a) K. Takimiya, T. Otsubo, Phosphorus Sulfur Silicon Relat. Elem. 2005, 180, 873-881;
    • (2005) Phosphorus Sulfur Silicon Relat. Elem , vol.180 , pp. 873-881
    • Takimiya, K.1    Otsubo, T.2
  • 27
    • 85163239656 scopus 로고    scopus 로고
    • T. Otsubo, K. Takimiya in TTF Chemistry - Fundamentals and Applications of Tetrathiafulvalene: Selenium Analogues of TTFs (Eds: J. Yamada, T. Sugimoto), Kodansha & Springer, Tokyo, 2004, chapter 5 and references cited therein.
    • b) T. Otsubo, K. Takimiya in TTF Chemistry - Fundamentals and Applications of Tetrathiafulvalene: Selenium Analogues of TTFs (Eds: J. Yamada, T. Sugimoto), Kodansha & Springer, Tokyo, 2004, chapter 5 and references cited therein.
  • 30
    • 85163238168 scopus 로고    scopus 로고
    • For examples of CSe2-free synthesis of TSeFs see: a Y. A. Jackson, C. L. White, M. V. Lakshmikantham, M. P. Cava, Tetrahedron Lett. 1987, 28, 5635-5636;
    • 2-free synthesis of TSeFs see: a) Y. A. Jackson, C. L. White, M. V. Lakshmikantham, M. P. Cava, Tetrahedron Lett. 1987, 28, 5635-5636;
  • 36
    • 85163239172 scopus 로고    scopus 로고
    • The LUMOs of the donor molecules, DIEDSS and DIETSe, were calculated by the MNDO-PM3 method using WinMOPAC ver. 3.5 Fujitsu Ltd
    • The LUMOs of the donor molecules, DIEDSS and DIETSe, were calculated by the MNDO-PM3 method using WinMOPAC ver. 3.5 (Fujitsu Ltd.).
  • 42
    • 85163239653 scopus 로고    scopus 로고
    • SAINT, Version 6.45, Bruker AXS. 2003
    • SAINT, Version 6.45, Bruker AXS. 2003.
  • 45
    • 33845935728 scopus 로고    scopus 로고
    • Version 5.03, Siemens Energy & Automation, Inc, Analytical Instrumentation, Madison, WI, USA
    • SHELXTL Reference Manual, Version 5.03, Siemens Energy & Automation, Inc., Analytical Instrumentation, Madison, WI, USA, 1996.
    • (1996) SHELXTL Reference Manual


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.