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Volumn 12, Issue 29, 2006, Pages 7652-7667

Anion binding versus intramolecular hydrogen bonding in neutral macrocyclic amides

Author keywords

Amides; Anion binding; Hydrogen bonds; Macrocyclic ligands; Receptors

Indexed keywords

AMIDES; ANION BINDING; MACROCYCLIC LIGANDS; RECEPTORS;

EID: 33750029269     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200501471     Document Type: Article
Times cited : (69)

References (70)
  • 7
    • 0038511082 scopus 로고    scopus 로고
    • For a review on macrocyclic anion receptors based on hydrogen-bonding interactions, see : K. Choi, A. D. Hamilton, Coord. Chem. Rev. 2003, 240, 101-110.
    • (2003) Coord. Chem. Rev. , vol.240 , pp. 101-110
    • Choi, K.1    Hamilton, A.D.2
  • 12
    • 0025989335 scopus 로고
    • Similar behaviour of bis-amide receptors was observed earlier by Hamilton et al. with respect to uncharged hydrogen-bond acceptors: S.-K. Chang, D. Van Engen, E. Fan, A. D. Hamilton, J. Am. Chem. Soc. 1991, 113, 7640-7645.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7640-7645
    • Chang, S.-K.1    Van Engen, D.2    Fan, E.3    Hamilton, A.D.4
  • 14
    • 0005927336 scopus 로고
    • A 20-membered macrocyclic tetraamide devoid of tert-butyl groups was already synthesized from isophtahlic acid chloride and 1,3-diaminopropane; however, its anion-binding properties were not studied. L. Wambach, F. Voegtle, Tetrahedron Lett. 1985, 26, 1483-1486.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 1483-1486
    • Wambach, L.1    Voegtle, F.2
  • 16
    • 0007964602 scopus 로고
    • From 2,6-pyridinedicarboxylic acid chloride and 1,4-diaminobutane: K. Krakowiak, Pol. J. Chem. 1988, 62, 231-233.
    • (1988) Pol. J. Chem. , vol.62 , pp. 231-233
    • Krakowiak, K.1
  • 17
    • 0001349811 scopus 로고
    • From 2,6-pyridinedicarboxylic acid chloride and 1,5-diaminopentane: K. Krakowiak, Pol. J. Chem. 1986, 60, 277-281.
    • (1986) Pol. J. Chem. , vol.60 , pp. 277-281
    • Krakowiak, K.1
  • 18
    • 0344327070 scopus 로고    scopus 로고
    • From 1,2-diaminobenzene and both isophthalic acid chloride and 2,6-pyridinedicarboxylic acid chloride: Z. Mo, W. Yang, J. Gao, H. Chen, J. Kang, Synth. Commun. 1999, 12, 2147-2153.
    • (1999) Synth. Commun. , vol.12 , pp. 2147-2153
    • Mo, Z.1    Yang, W.2    Gao, J.3    Chen, H.4    Kang, J.5
  • 28
    • 33750020755 scopus 로고    scopus 로고
    • See reference [9] and references therein
    • See reference [9] and references therein.
  • 33
    • 0005814886 scopus 로고    scopus 로고
    • A similar twist of the amide group was calculated earlier for benzamides: M. Čajan, I. Stibor, J. Koča, J. Phys. Chem. A 1999, 103, 3778-3782.
    • (1999) J. Phys. Chem. A , vol.103 , pp. 3778-3782
    • Čajan, M.1    Stibor, I.2    Koča, J.3
  • 37
    • 33750033108 scopus 로고    scopus 로고
    • note
    • The AM1 method has been recently successfully applied to much larger systems containing isophthalamide units.
  • 38
    • 33749991986 scopus 로고    scopus 로고
    • note
    • The only exceptions are found in the largest macrocycle 8, for example, SS(+,-)SS(+,-) conformations nos. 526 and 647, see Supporting Information.
  • 40
    • 33749999369 scopus 로고    scopus 로고
    • note
    • - complex grown in the presence of an excess of tetrabutylammonium fluoride, see reference [32].
  • 44
    • 0037007932 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2002, 41, 2335-2338.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2335-2338
  • 49
    • 33749993907 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 59, 3348-3391.
    • (2000) Angew. Chem. Int. Ed. , vol.59 , pp. 3348-3391
  • 61
    • 4544353066 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 1222-1224.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 1222-1224
  • 66
    • 0037715341 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 2738-3740.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 2738-3740


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.