Abstract
The kinetics of reduction of tetrachloroaurate(III) by glycine has been spectrophotometrically studied in NaOAc–AcOH buffer in the pH range 3.73–4.77. The reaction is first order with respect to both Au(III) and glycine. Both H+ and Cl− ions have inhibiting effects on the reaction rate. The rate decreases with a decrease in the dielectric constant of the medium. AuCl −4 and AuCl3(OH)− are presumed to be the predominant oxidizing species under the conditions of the experiment. The reaction of gold(III) and zwitterionic species of glycine proceeds with the intermediate formation of gold(I) and iminic cation and the latter subsequently hydrolyses in a fast step to produce formaldehyde and ammonium ion. Formaldehyde was identified as the only organic product by 1H NMR spectroscopy.
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References
Shaw CF III (1979) Perspect Biol Med 2:287
Sadler PJ (1976) Struct Bonding (Berlin) 29:171
Dash KC, Schmidbaur H (1983) Met Ions Biol Syst 14:180
Sadler PJ, Sue RE (1994) Met Based Drugs 1:107
Gleichmann E, Schuhmann D, Kubickamurauyi M (1990) Eur J Pharmacol 183:78
Parish RV, Howe BP, Wright JP, Mack J, Prichard RG, Buckley RG, Elsome AM, Fricker SP (1996) Inorg Chem 35:1659
Calamai P, Carotti S, Gherri A, Mazzei T, Messori L, Mini E, Orioli P, Speroni GP (1998) Anticancer Drug Des 13:67
Che C (2004) PCT Int Appl 80
Sen PK, Bilkis AB, Sen Gupta KK (1998) Int J Chem Kinet 30:613
Pal B, Sen PK, Sen Gupta KK (2001) J Phys Org Chem 14:284
Sen Gupta KK, Pal B, Sen PK (1999) Int J Chem Kinet 31:873
Canumalla AJ, Al-Zamil N, Phillips M, Isab AA, Shaw III CF (2001) J Inorg Biochem 85:67
Fukuzumi S, Ohkubo K, Wenbo E, Ou Z, Shao J, Kadish KM, Hutchison JA, Ghiggino KP, Sintic PJ, Crossley MJ (2003) J Am Chem Soc 125:14984
Marcon G, Messori L, Orioli P, Cinellu MA, Mingheetti G (2003) Eur J Biochem 270:4655
Insausti MJ, Mata-Perez F, Alvarez-Macho MP (1995) Int J Chem Kinet 27:507
Arrizabalaga A, Andres-Ordax FJ, Fernandez-Aranguiz MY, Peche R (1996) Int J Chem Kinet 28:799
Choubey M, Pandey A (1999) Oxid Commun 22:293
Kumar A, Kumar P, Ramamurthy P (1999) Polyhedron 18:773
Katre YR, Solanki SK, Patil S, Joshi GK (2005) Asian J Chem 17:423
Sarathi TVNP, Kumar AK, Kishore KK, Vani P (2005) J Chem Sci(India) 117:329
Pal B, Sen PK, Sen Gupta KK (2006) J Indian Chem Soc 83:762
Rich LR, Taube H (1954) J Phys Chem 58:1
Fry FH, Hamilton GA, Turkevich J (1966) Inorg Chem 5:1943
Robb W (1967) Inorg Chem 6:382
Bekker PV, Louw WJ, Robb W (1972) Inorg Nucl Chem Lett 8:849
Moodley KG, Nicol MJ (1977) J Chem Soc Dalton Trans 993
Zou J, Guo Z, Parkinson JA, Chen Y, Sadler PJ (1999) Chem Commun 1359
Owen BB (1934) J Am Chem Soc 56:24
Devra V, Jain S, Sharma PD (1994) Int J Chem Kinet 26:577
Ramachandran MS, Easwaramoorthy D, Malim Manira RP (1996) Int J Chem Kinet 28:545
Sherigara BS, Ishwar Bhat K, Pinto I, Made Gowda NM (1995) Int J Chem Kinet 27:675
Arrizabalaga A, Andres-Ordax FJ, Fernandez-Aranguiz MY, Peche R (1996) Int J Chem Kinet 28:799
March J (1985) Advanced organic chemistry: reaction mechanism and structure. John Wiley & Sons, New York, p 784
Nalwaya N, Jain A, Hiran BL (2002) J Indian Chem Soc 79:587
Hassan RM (1991) Can J Chem 69:2018
Hassan M, Mousa MA, Wahdan MH (1988) J Chem Soc Dalton Trans 605
Hussain MY, Ahmad F (1990) Transition Met Chem 15:185
Sen PK, Sanyal A, Sen Gupta KK (1996) Bull Chem Soc Jpn 69:1543
Maritz BS, van Eldik R (1976) Inorg Chim Acta 17:21
Bekker PVZ, Louw WJ, Robb W (1972) Inorg Chim Acta 6:564
Louw WJ, Robb W (1969) Inorg Chim Acta 3:303
Louw WJ, Robb W (1974) Inorg Chim Acta 8:253
Laidler KJ (1987) Chemical kinetics 3rd edn. Harper Row, New York, p 195
Vogel AI (1958) Elementary practical organic chemistry (part III) quantitative organic analysis. Longmans, London, pp 709–710
Feigl F (1956) Spot tests in organic analysis. Elsevier, Amsterdam, pp 434, 469
Buckingham J (ed) (1982) Dictionary of organic compounds, 5th edn, vol. 3. Chapman & Hall, New York, p 2676
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Thanks are due to Dr. S. Bhar, Department of Chemistry, Jadavpur University for helpful discussions.
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Sen, P.K., Gani, N., Midya, J.K. et al. Kinetics and mechanism of the reduction of gold(III) by glycine in acetate buffer. Transition Met Chem 33, 229–236 (2008). https://doi.org/10.1007/s11243-007-9019-x
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DOI: https://doi.org/10.1007/s11243-007-9019-x