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Volumn 129, Issue 1, 2007, Pages 48-58

Structural criteria for the design of anion receptors: The interaction of halides with electron-deficient arenes

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEXATION; CRYSTAL STRUCTURE; HYDROGEN BONDS; NEGATIVE IONS;

EID: 33846066355     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja063460m     Document Type: Article
Times cited : (294)

References (70)
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    • Related charge-insulator complexes, in which an aromatic ring is sandwiched between an anion and a metal cation, lie outside the scope of the present study. For theoretical studies, see: a
    • Related charge-insulator complexes, in which an aromatic ring is sandwiched between an anion and a metal cation, lie outside the scope of the present study. For theoretical studies, see: (a) Garau, C.; Quinoñero, D.; Frontera, A.; Ballester, P.; Costa, A.; Deyà, P. M. New J. Chem. 2003, 2, 211.
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    • For representative solid-state examples, see: d
    • For representative solid-state examples, see: (d) Fairchild, R. M.; Holman, K. T. J. Am. Chem. Soc. 2005, 127, 16364.
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    • Fairchild, R.M.1    Holman, K.T.2
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    • Single-crystal X-ray structures also provide examples of anions interacting with charged π systems in which electron-deficient aromatic rings are coordinated to metal cations: (a) de Hoog, P, Gamez, P, Mutikainen, I, Turpeinen, U, Reedijk, J. Angew. Chem, Int. Ed. 2004, 43, 5815
    • Single-crystal X-ray structures also provide examples of anions interacting with charged π systems in which electron-deficient aromatic rings are coordinated to metal cations: (a) de Hoog, P.; Gamez, P.; Mutikainen, I.; Turpeinen, U.; Reedijk, J. Angew. Chem., Int. Ed. 2004, 43, 5815.
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    • 5 substituents are present: (a) Maeda, H.; Osuka, A.; Furuta, H. J. Inclusion Phenom. Macrocycl. Chem. 2004, 49, 33:
    • 5 substituents are present: (a) Maeda, H.; Osuka, A.; Furuta, H. J. Inclusion Phenom. Macrocycl. Chem. 2004, 49, 33:
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    • For an example of an aryl sulfonate interacting with a neutral arene, see: c
    • For an example of an aryl sulfonate interacting with a neutral arene, see: (c) Schneider, H. J.; Werner, F.; Blatter, T. J. Phys. Org. Chem. 1993, 6, 590.
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    • 3 In fact, the actual criterion used in those studies was the sum of van der Waals radii + 1.0 Å, which is the default option provided in the Quest Version 5 database searching program: Garau, C. Personal communication, February, 2006.
    • 3 In fact, the actual criterion used in those studies was the sum of van der Waals radii + 1.0 Å, which is the default option provided in the Quest Version 5 database searching program: Garau, C. Personal communication, February, 2006.
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    • Such complexes were first reported in: (a) Jackson, C. J.; Gazzolo F. H. J. Am. Chem. Soc. 1900, 23, 376.
    • Such complexes were first reported in: (a) Jackson, C. J.; Gazzolo F. H. J. Am. Chem. Soc. 1900, 23, 376.
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    • A structure was later isolated and characterized in: (b) Meisenheimer, J. Justus Liebigs Ann. Chem. 1902, 323, 205.
    • A structure was later isolated and characterized in: (b) Meisenheimer, J. Justus Liebigs Ann. Chem. 1902, 323, 205.
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    • -.
    • -.
  • 69
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    • We do not observe a preference for the union to he located over the para-position. Possible explanations include (i) electrostatic attraction between the anion and metal cation and (ii) the electropositive metal center inductively stabilizing anion binding at the ortho-positions more than at the para-position
    • We do not observe a preference for the union to he located over the para-position. Possible explanations include (i) electrostatic attraction between the anion and metal cation and (ii) the electropositive metal center inductively stabilizing anion binding at the ortho-positions more than at the para-position.
  • 70
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    • -1 (Table 2).
    • -1 (Table 2).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.