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Volumn 44, Issue 1, 2004, Pages 87-91

Molecular loop lock: A redox-driven molecular machine based on a host-stabilized charge-transfer complex

Author keywords

Charge transfer; Electrochemistry; Molecular devices; Self assembly; Supramolecular chemistry

Indexed keywords

NAPHTHALENE; PARAQUAT; SODIUM DITHIONITE;

EID: 11244351588     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200461806     Document Type: Article
Times cited : (153)

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    • 2⊂CB[8]) and free CB[8] upon chemical or electrochemical reduction and that the reaction is reversible: W. S. Jeon, H.-J. Kim, C. Lee, K. Kim, Chem. Commun. 2002, 1828.
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    • note
    • 2+ generated in the first reduction step, but we do not clearly understand this process at the moment.
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    • note
    • The bulky cationic unit was introduced at the terminal to prevent the formation of intermolecular CT complexes and intermolecular viologen radical-cation dimers inside CB[8] upon reduction. Another role of the cationic terminal unit is to improve the solubility of the complex after reduction.
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    • note
    • 3+ (see Supporting Information).
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    • 2+) and the activation process (reduction).
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    • note
    • 3+ and related compounds will be published elsewhere in due course.
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    • (Ed.: H. S. Nalwa), American Scientific, California
    • It may also be viewed as a reversibly operating molecular AND logic gate: F. M. Raymo, S. Giordani in Encyclopedia of Nanoscience and Nanotechnology, Vol. 5 (Ed.: H. S. Nalwa), American Scientific, California, 2004, pp. 677-692.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.