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Volumn 12, Issue 4, 2006, Pages 1144-1155

Electron-rich tetrathiafuvalene-triarylamine conjugates: Synthesis and redox properties

Author keywords

Conducting materials; Cyclic voltammetry; Hole transfer; Tetrathiafulvalene; Triarylamines

Indexed keywords

AMORPHOUS MATERIALS; CYCLIC VOLTAMMETRY; DIFFERENTIAL SCANNING CALORIMETRY; ELECTROCHEMISTRY; REDOX REACTIONS; SYNTHESIS (CHEMICAL);

EID: 31344436671     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200500928     Document Type: Article
Times cited : (19)

References (80)
  • 2
    • 10244244991 scopus 로고    scopus 로고
    • a) See the special issue on molecular conductors: Chem. Rev. 2004. 104, 4887-5781;
    • (2004) Chem. Rev. , vol.104 , pp. 4887-5781
  • 16
    • 10244264738 scopus 로고    scopus 로고
    • and references therein
    • M. Fourmigu, P. Batail, Chem. Rev. 2004, 104, 5379, and references therein.
    • (2004) Chem. Rev. , vol.104 , pp. 5379
    • Fourmigu, M.1    Batail, P.2
  • 73
    • 0003464216 scopus 로고    scopus 로고
    • (Eds.: P. J. Linstrom, W. G. Mallard). National Institute of Standards and Technology. Gaithersburg MD. 20899. June
    • The ionisation potential (IP) of triphenylamine was reported to be 6.8 eV, as estimated from gas-phase ultraviolet photoelectron spectroscopy (UV-PES). However, the IP (or HOMO) of condensed triarylamines is much lower. See: a) NIST Chemistry Wek Book, NIST Standard Reference Database Number 69 (Eds.: P. J. Linstrom, W. G. Mallard). National Institute of Standards and Technology. Gaithersburg MD. 20899. June 2005 (http://webbook.nist.gov);
    • (2005) NIST Chemistry Wek Book, NIST Standard Reference Database Number 69 , vol.69
  • 76
    • 31344472693 scopus 로고    scopus 로고
    • available from the web as article in press
    • S. Amthor, C. Lambert, Chem. Phys. 2005, available from the web as article in press.
    • (2005) Chem. Phys.
    • Amthor, S.1    Lambert, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.