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Volumn 36, Issue 25, 1997, Pages 5777-5784

Weak Interactions in Ternary Copper(II) Complexes with lodotyrosinates. Biological Significance of the Iodines in Thyroid Hormones

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EID: 0000108910     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic9705397     Document Type: Article
Times cited : (52)

References (68)
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    • note
    • 2tyr with the deprotonated diiodophenol moiety; Phe, phenylalaninate; Ala, alaninate; DA, aromatic diamine; phen, 1,10-phenanthroline; bpy, 2,2′-bipyridine; ampy, 2-(aminomethyl)pyridine; hista, histamine; en, ethylenediamine.
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    • Dielectric constants for the solvents were obtained from the literature: (a) Åkerlöf, G. J. Am. Chem. Soc. 1932, 54, 4125-4139. (b) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1936, 58, 1241-1243. (c) Critchfield, F. E.; Gibson, J. A., Jr.; Hall, J. L. J. Am. Chem. Soc. 1953, 75, 1991-1992. (d) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1953, 75, 6357. (e) Sigel, H.; Malini-Balakrishnan, R.; Häring, U. K. J. Am. Chem. Soc. 1985, 107, 5137-5148.
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    • Dielectric constants for the solvents were obtained from the literature: (a) Åkerlöf, G. J. Am. Chem. Soc. 1932, 54, 4125-4139. (b) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1936, 58, 1241-1243. (c) Critchfield, F. E.; Gibson, J. A., Jr.; Hall, J. L. J. Am. Chem. Soc. 1953, 75, 1991-1992. (d) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1953, 75, 6357. (e) Sigel, H.; Malini-Balakrishnan, R.; Häring, U. K. J. Am. Chem. Soc. 1985, 107, 5137-5148.
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    • Dielectric constants for the solvents were obtained from the literature: (a) Åkerlöf, G. J. Am. Chem. Soc. 1932, 54, 4125-4139. (b) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1936, 58, 1241-1243. (c) Critchfield, F. E.; Gibson, J. A., Jr.; Hall, J. L. J. Am. Chem. Soc. 1953, 75, 1991-1992. (d) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1953, 75, 6357. (e) Sigel, H.; Malini-Balakrishnan, R.; Häring, U. K. J. Am. Chem. Soc. 1985, 107, 5137-5148.
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    • Dielectric constants for the solvents were obtained from the literature: (a) Åkerlöf, G. J. Am. Chem. Soc. 1932, 54, 4125-4139. (b) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1936, 58, 1241-1243. (c) Critchfield, F. E.; Gibson, J. A., Jr.; Hall, J. L. J. Am. Chem. Soc. 1953, 75, 1991-1992. (d) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1953, 75, 6357. (e) Sigel, H.; Malini-Balakrishnan, R.; Häring, U. K. J. Am. Chem. Soc. 1985, 107, 5137-5148.
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    • Dielectric constants for the solvents were obtained from the literature: (a) Åkerlöf, G. J. Am. Chem. Soc. 1932, 54, 4125-4139. (b) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1936, 58, 1241-1243. (c) Critchfield, F. E.; Gibson, J. A., Jr.; Hall, J. L. J. Am. Chem. Soc. 1953, 75, 1991-1992. (d) Åkerlof, G.; Short, O. A. J. Am. Chem. Soc. 1953, 75, 6357. (e) Sigel, H.; Malini-Balakrishnan, R.; Häring, U. K. J. Am. Chem. Soc. 1985, 107, 5137-5148.
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    • note
    • -. The distances of N(1), C(1), N(2), C(2), and C(3) atoms from the ring are 3.53, 3.53, 4.04, 4.39, and 4.05 Å for A and 3.65, 3.41, 3.91, 4.54, and 4.33 Å for B, respectively. The differences between the corresponding distances for A and B are 0.12, -0.12, -0.13, 0.15, and 0.28 Å, respectively.
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    • The values in Table 5 were obtained by analyzing the corresponding crystal structural data
    • The values in Table 5 were obtained by analyzing the corresponding crystal structural data.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.