메뉴 건너뛰기




Volumn 115, Issue 3, 2011, Pages 785-790

Multidecker bis(benzene)chromium: Opportunities for design of rigid and highly flexible molecular wires

Author keywords

[No Author keywords available]

Indexed keywords

[2.2]PARACYCLOPHANE; BENZENE RING; BIPHENYLENE; CONFORMATIONAL FLEXIBILITY; DENSITY FUNCTIONAL THEORY CALCULATIONS; ELECTRON RULES; ELECTRONICS APPLICATIONS; FERMI ENERGY; HIGH CONDUCTIVITY; HIGHEST OCCUPIED MOLECULAR ORBITAL; HOMO ENERGIES; INJECTED ELECTRONS; METAL ELECTRODES; MOLECULAR WIRES; MONOMER UNITS; ORBITALS; SANDWICH COMPLEXES; SUB-BANDS;

EID: 78751672839     PISSN: 19327447     EISSN: 19327455     Source Type: Journal    
DOI: 10.1021/jp109782q     Document Type: Article
Times cited : (20)

References (72)
  • 44
    • 84982624480 scopus 로고
    • The pyrolysis of biphenyl at 420-465 °C produces benzene, terphenyls, and quaterphenyls, over an activation barrier of 72.1 kcal/mol as found by
    • The pyrolysis of biphenyl at 420-465 °C produces benzene, terphenyls, and quaterphenyls, over an activation barrier of 72.1 kcal/mol as found by: Proksch, E.; Strigl, A.; Wagner-Loeffler, M.; Szinovatz, W. Chem. Ing. Tech. 1985, 57, 148
    • (1985) Chem. Ing. Tech. , vol.57 , pp. 148
    • Proksch, E.1    Strigl, A.2    Wagner-Loeffler, M.3    Szinovatz, W.4
  • 45
    • 0030577017 scopus 로고    scopus 로고
    • With regard to biphenylene, it is produced as a minor product in flash vacuum pyrolysis of 9,10-didehydrophenanthrene at 1100 °C (the major product is phenanthrene) as found by
    • With regard to biphenylene, it is produced as a minor product in flash vacuum pyrolysis of 9,10-didehydrophenanthrene at 1100 °C (the major product is phenanthrene) as found by: Brown, R. F. C.; Coulston, K. J.; Eastwood, F. W. Tetrahedron Lett. 1996, 37, 6819
    • (1996) Tetrahedron Lett. , vol.37 , pp. 6819
    • Brown, R.F.C.1    Coulston, K.J.2    Eastwood, F.W.3
  • 46
    • 78751665182 scopus 로고    scopus 로고
    • Under these conditions, biphenylene was converted to only a small extent to cyclopent[ a ]indene and acenapthylene
    • Under these conditions, biphenylene was converted to only a small extent to cyclopent[ a ]indene and acenapthylene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.