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Volumn 137, Issue 1, 2015, Pages 499-507

Evidence for halogen bond covalency in acyclic and interlocked halogen-bonding receptor anion recognition

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; BINDING ENERGY; CHARGE TRANSFER; CHLORINE; HYDROGEN BONDS; IONS; TRANSITION METALS; X RAY ABSORPTION SPECTROSCOPY; X RAY CRYSTALLOGRAPHY;

EID: 84921047897     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja511648d     Document Type: Article
Times cited : (189)

References (84)
  • 84
    • 84907485027 scopus 로고    scopus 로고
    • Hunter and co-workers have recently demonstrated that the halogen bond formed between tetramethylthiourea and molecular iodine is insensitive to the nature of the organic solvent, where association constants determined in alkanes and alcohols are similar in magnitude, suggesting charge transfer interactions are making a significant contribution to the halogen bond. See
    • Hunter and co-workers have recently demonstrated that the halogen bond formed between tetramethylthiourea and molecular iodine is insensitive to the nature of the organic solvent, where association constants determined in alkanes and alcohols are similar in magnitude, suggesting charge transfer interactions are making a significant contribution to the halogen bond. See: Robertson, C. C.; Perutz, R. N.; Brammer, L.; Hunter, C. A. Chem. Sci. 2014, 5, 4179-4183
    • (2014) Chem. Sci. , vol.5 , pp. 4179-4183
    • Robertson, C.C.1    Perutz, R.N.2    Brammer, L.3    Hunter, C.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.