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Volumn 37, Issue 7, 1998, Pages 932-935

Stereospecificity and self-selectivity in the generation of a chiral molecular tetrahedron by metal-assisted self-assembly

Author keywords

Chirality; Gallium; Self assembly; Supramolecular chemistry

Indexed keywords


EID: 0031971174     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19980420)37:7<932::AID-ANIE932>3.0.CO;2-C     Document Type: Article
Times cited : (117)

References (52)
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    • note
    • w) = 0.073(0.069).
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    • w) = 0.061(0.056). TMI = tetramethyldihydroimidazolinium.
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    • note
    • 6-, but none are anticipated for these complexes. A less symmetric species is also unlikely as it would be expected that the various methyl and methylene protons of the ligand backbone would have very different chemical environments.
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    • 12- (0 ≤ a ≤ 6). If more than one of each enantiomer is present in a metal complex (2 ≤ a ≤ 4), these ligands can be arranged in multiple orientations relative to each other. A list of all possible isomers is given in the supporting information on the WWW.
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    • Other examples of self-selectivity in self-assembly: R. Krämer, J.-M. Lehn, A. Marquis-Rigault, Proc. Natl. Acad. Sci. USA 1993, 90, 5394-5398; D. L. Caulder, K. N. Raymond, Angew. Chem. 1997, 109, 1508-1510; Angew. Chem. Int. Ed. Engl. 1997, 36, 1439-1442; M. A. Masood, E. J. Enemark, T. D. P. Stack, ibid. 1998, 110, 973-977 and 1998, 37, 928-932.
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    • Other examples of self-selectivity in self-assembly: R. Krämer, J.-M. Lehn, A. Marquis-Rigault, Proc. Natl. Acad. Sci. USA 1993, 90, 5394-5398; D. L. Caulder, K. N. Raymond, Angew. Chem. 1997, 109, 1508-1510; Angew. Chem. Int. Ed. Engl. 1997, 36, 1439-1442; M. A. Masood, E. J. Enemark, T. D. P. Stack, ibid. 1998, 110, 973-977 and 1998, 37, 928-932.
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    • Other examples of self-selectivity in self-assembly: R. Krämer, J.-M. Lehn, A. Marquis-Rigault, Proc. Natl. Acad. Sci. USA 1993, 90, 5394-5398; D. L. Caulder, K. N. Raymond, Angew. Chem. 1997, 109, 1508-1510; Angew. Chem. Int. Ed. Engl. 1997, 36, 1439-1442; M. A. Masood, E. J. Enemark, T. D. P. Stack, ibid. 1998, 110, 973-977 and 1998, 37, 928-932.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1439-1442
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    • 0027172787 scopus 로고    scopus 로고
    • Other examples of self-selectivity in self-assembly: R. Krämer, J.-M. Lehn, A. Marquis-Rigault, Proc. Natl. Acad. Sci. USA 1993, 90, 5394-5398; D. L. Caulder, K. N. Raymond, Angew. Chem. 1997, 109, 1508-1510; Angew. Chem. Int. Ed. Engl. 1997, 36, 1439-1442; M. A. Masood, E. J. Enemark, T. D. P. Stack, ibid. 1998, 110, 973-977 and 1998, 37, 928-932.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.110 , pp. 973-977
    • Masood, M.A.1    Enemark, E.J.2    Stack, T.D.P.3
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    • 0031971605 scopus 로고    scopus 로고
    • Other examples of self-selectivity in self-assembly: R. Krämer, J.-M. Lehn, A. Marquis-Rigault, Proc. Natl. Acad. Sci. USA 1993, 90, 5394-5398; D. L. Caulder, K. N. Raymond, Angew. Chem. 1997, 109, 1508-1510; Angew. Chem. Int. Ed. Engl. 1997, 36, 1439-1442; M. A. Masood, E. J. Enemark, T. D. P. Stack, ibid. 1998, 110, 973-977 and 1998, 37, 928-932.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 928-932
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    • note
    • AM1 calculations were performed with an idealized isopropylformamide unit.
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    • note
    • pr.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.