Carboxy ester hydrolysis promoted by a dicopper(II) macrocylic polyamine complex with hydroxypropyl pendant groups

European Journal of Inorganic Chemistry

Volumn , Issue 9, 2004, Pages 1894-1901

  Huang, Jin ^a   Li, Shu An ^a   Li, Dong Feng ^a   Yang, De Xi ^a   Sun, Wei Yin ^a   Tang, Wen Xia ^a  

^a NANJING UNIVERSITY   (China)

Author keywords

Copper; Hydrolysis; Macrocyclic ligands; Mass spectrometry; Potentiometric titrations

Indexed keywords

CATALYST ACTIVITY; COPPER; COPPER COMPOUNDS; ESTERS; LIGANDS; MASS SPECTROMETRY; POTENTIOMETERS (ELECTRIC MEASURING INSTRUMENTS); RATE CONSTANTS; TITRATION; VOLTAMMETRY;

DICOPPER; DINUCLEAR; ESTER HYDROLYSIS; MACRO-CYCLIC LIGANDS; MACROCYCLES; ORTHORHOMBIC SPACE GROUPS; PENDANT GROUPS; POLYAMINES; POTENTIOMETRIC TITRATIONS; SYNTHESISED;

HYDROLYSIS;

ACETIC ACID DERIVATIVE; COPPER COMPLEX; ESTER DERIVATIVE; HYDROXYL GROUP; LIGAND; MACROCYCLIC COMPOUND; POLYAMINE DERIVATIVE; PROPANE;

ACIDITY; ARTICLE; CATALYSIS; CHEMICAL COMPOSITION; CRYSTAL STRUCTURE; HYDROLYSIS; PH; POTENTIOMETRIC TITRATION; PROTON TRANSPORT; SYNTHESIS;

EID: 4544295274     PISSN: 14341948     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejic.200300452     Document Type: Article

References (19)

1. [1a] A. E. Eriksson, T. A. Jones, A. Liljas, Proteins: Struc. Funct. Gen. 1988, 4, 274-282.
2. [1b] S. K. Nair, D. W. Christianson, J. Am. Chem. Soc. 1991, 113, 9455-9458.
3. D. W. Christianson, W. N. Lipscomb, Acc. Chem. Res. 1989, 22, 62-69.
4. K. A. Deal, J. N. Burstyn, Inorg. Chem. 1996, 35, 2792-2798.
5. E. Kimura, I. Nakamura, T. Koike, M. Shionaoya, Y. Kodama, T. Ikeda, T. Shiro, J. Am. Chem. Soc. 1994, 116, 4764-4771.
6. T. Koile, S. Kajitan, I. Nakamura, E. Kimura, M. Shiro, J. Am. Chem. Soc. 1995, 117, 1210-1219.
7. M. J. Young, D. Wajnon, R. C. Hynes, J. Chin, J. Am. Chem. Soc. 1995, 117, 9441-9447.
8. E. L. Mutterties, L. J. Guggenberger, J. Am. Chem. Soc. 1974, 96, 1748-1756.
9. J. Galy, J. I. Bonnet, S. Anderson, Acta Chem. Scand., Ser. A 1979, 33, 383-389.
10. S. A. Li, J. Xia, D. X. Yang, Y. Xu, D. F. Li, M. F. Wu, W. X. Tang, Inorg. Chem. 2002, 42, 1807-1815.
11. J. Xia, Y. Xu, S. A. Li, K. B. Yu, W. X. Tang, Inorg. Chem. 2001, 40, 2394-2401.
12. C. Bazzicalpi, A. Bencini, E. Berni, A. Bianchi, V. Fedi, V. Fusi, C. Giorgi, P. Paoletti, B. Valtancoli, Inorg. Chem. 1999, 38, 4115-4122.
13. S. A. Li, D. X. Yang, D. F. Li, J. Huang, W. X. Tang, New. J. Chem. 2002, 26, 1831-1837.
14. Dow Chemical Co. Fr. 2112697, 1972-07-28; from Chem. Abstr. 1973, 78, 124002g).
15. SAINT, version 4.0, Data Integration Software, Bruker AXS, Inc., Madison, WI, 1997.
16. G. M. Sheldrick, SADABS, version 2.01, Empirical Absorption Correction Program, University of Göttingen, 1996.
17. G. M. Sheldrick, SHELXTL, version 5.10, Program for Crystal Structure Determinations, Siemens Industrial Automation, Inc., Madison, WI, 1997.
18. A. E. Martell, R. J. Motekaitis, Determination and uses of stability constants, 2nd ed., VCH, New York, 1989.
19. E. Kimura, E. Kikuta, J. Biol. Inorg. Chem. 2000, 5, 139.