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Volumn 17, Issue 26, 2011, Pages 7236-7250

Conformationally controlled electron delocalization in n-type rods: Synthesis, structure, and optical, electrochemical, and spectroelectrochemical properties of dicyanocyclophanes

Author keywords

conjugation; cyanides; cyclophanes; electrochemistry; medium ring compounds

Indexed keywords

CONFORMATIONAL RIGIDITY; CONJUGATION; CYCLOPHANES; DOMINANT FACTOR; ELECTRON DELOCALIZATION; MEDIUM-RING COMPOUNDS; MODEL COMPOUND; MOLECULAR CONFORMATION; N-TYPE SEMICONDUCTORS; PACKING PROPERTIES; QUANTUM-MECHANICAL CALCULATION; RADICAL ANIONS; REDUCTION PROCESS; SOLID-STATE STRUCTURES; SPECTROELECTROCHEMICAL; SPECTROELECTROCHEMICAL INVESTIGATIONS; SPECTROELECTROCHEMICAL PROPERTIES; STRUCTURAL FEATURE; SYSTEMATIC CORRELATION; TORSION ANGLE; TWO-STEP REDUCTION; VERTICAL EXCITATION ENERGY; X RAY CRYSTAL STRUCTURES;

EID: 79958853032     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201003763     Document Type: Article
Times cited : (24)

References (92)
  • 7
    • 70449116077 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 8886-8890
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 8886-8890
  • 59
    • 79958857196 scopus 로고    scopus 로고
    • HOMO and LUMO levels of the dithiolcyclophane counterparts were calculated for comparison using similar DFT methods
    • HOMO and LUMO levels of the dithiolcyclophane counterparts were calculated for comparison using similar DFT methods.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.