Reactivity of neonicotinoid pesticides with singlet oxygen

Catalysis Today

Volumn 151, Issue 1-2, 2010, Pages 137-142

  Dell'Arciprete, M L ^a   Santos Juanes, L ^b   Arques, A ^b   Vercher, R F ^b   Amat, A M ^b   Furlong, J P ^c   Martire D O ^a   Gonzalez, M C ^a  

^a INSTITUTO DE INVESTIGACIONES FISICOQUÍMICAS TEÓRICAS Y APLICADAS INIFTA   (Argentina)

^b UNIVERSITAT POLITÈCNICA DE VALÈNCIA   (Spain)

^c FACULTAD DE CIENCIAS EXACTAS   (Argentina)

Author keywords

Neonicotinoids; Rose Bengal; Self cleaning; Singlet oxygen; Sunlight

Indexed keywords

6-CHLORONICOTINIC ACID; ABIOTIC PATHWAYS; CHARGE-TRANSFER REACTIONS; DEGRADATION PRODUCTS; EXCITED TRIPLET STATE; IMIDACLOPRIDS; NATURAL WATERS; NATURALLY OCCURRING; NEONICOTINOID INSECTICIDES; NEONICOTINOIDS; REACTION MECHANISM; ROSE BENGAL; SINGLET OXYGEN; TRIPLET STATE; VIBRIO FISCHERI;

CHARGE TRANSFER; DEGRADATION; INSECTICIDES; ION EXCHANGE; RATE CONSTANTS; REACTION KINETICS;

OXYGEN;

EID: 77953287424     PISSN: 09205861     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cattod.2010.01.020     Document Type: Article

References (25)

1. Matsuda K., Buckingham S.D., Kleier D., Rauh J.J., Grauso M., and Satelle D.B. Neonicotinoids: insecticides acting on insect nicotinic acetylcholine receptors. Trends Pharmacol. Sci. 22 (2001) 573-580
2. Iwasa T., Motoyama N., Ambrose J.T., and Roe R.M. Mechanism for the differential toxicity of neonicotinoid insecticides in the honey bee. Crop Prot. 23 (2004) 371-378
3. Piram A., Salvador A., Verne C., Herbreteau B., and Faure R. Photolysis of β-blockers in environmental waters. Chemosphere 73 (2008) 1265-1271
4. Dell'Arciprete M.L., Santos-Juanes L., Arques Sanz A., Vicente R., Amat A.M., Furlong J.P., Mártire D.O., and Gonzalez M.C. Reactivity of hydroxyl radicals with neonicotinoid insecticides: mechanism and changes in toxicity. Photochem. Photobiol. Sci. 8 (2009) 1016-1023
5. David Gara P., Bosio G.N., Arce V.B., Poulsen L., Ogilby P.R., Giudici R., Gonzalez M.C., and Martire D.O. Photoinduced degradation of the herbicide clomazone model reactions for natural and technical systems. Photochem. Photobiol. 85 (2009) 686-692
6. Zepp R.G., Wolfe N.L., Baughman G.L., and Hollis R.C. Singlet oxygen in natural waters. Nature 267 (1997) 421-423
7. g) production and quenching by hydroxybiphenyls. Chemosphere 26 (1993) 1691-1701
8. Barbieri Y., Massad W.A., Díaz D.J., Sanz J., Amat-Guerri F., and García N.A. Photodegradation of Bisphenol A and related compounds under natural-like conditions in the presence of riboflavin. Chemosphere 73 (2008) 564-571
9. Haag W.R., and Hoigné J. Singlet oxygen in surface waters. 3. Photochemical formation and steady-state concentrations in various types of waters. Environ. Sci. Technol. 20 (1986) 341-348
10. Wilkinson F., Helman W.P., and Ross A.B. Rate constants for the decay and reactions of the lowest electronically excited singlet state of molecular oxygen in solution. An expanded and revised compilation. J. Phys. Chem. Ref. Data 22 (1993) 663-1021
11. Lambert C.R., and Kochevar I.E. Electron transfer quenching of the rose bengal triplet state. Photochem. Photobiol. 66 (1997) 15-25
12. 2 photocatalysis. Appl. Catal. B 75 (2007) 229-238
13. Miller J.S. Rose bengal-sensitized photooxidation of 2-chlorophenol in water using solar simulated light. Water Res. 39 (2005) 412-422
14. Young R.H., Brewer D., Kayser R., Martin R., Feriozi D., and Keller R.A. The mechanism of quenching of singlet oxygen by amines-III. Evidence for a charge-transfer-like complex. Can. J. Chem. 52 (1974) 2889-2893
15. g) by amines and aromatic hydrocarbons. J. Phys. Chem. A 102 (1998) 9308
16. Hiller K.O., and Asmus K.D. Formation and reduction reactions of α-amino radicals derived from methionine and its derivatives in aqueous solutions. J. Phys. Chem. 87 (1983) 3682-3688
17. von Sonntag C., and Schuchmann H. In: Alfassi Z.B. (Ed). Peroxyl Radicals in the Chemistry of Free Radicals (1997), Wiley, Chichester 173
18. Baciocchi E., Del Giacco T., and Lapi A. Oxygenation of benzyldimethylamine by singlet oxygen. Products and mechanism. Org. Lett. 6 (2004) 4791-4794
19. Young R.H., and Brewer D.R. In: Ranby B., and Rabek J.F. (Eds). Singlet Oxygen Reactions with Organic Compounds and Polymers (1976) 36-43
20. Gonzalez M.C., Oliveros E., Wörner M., and Braun A.M. Vacuum ultraviolet photolysis of aqueous reaction systems. J. Photochem. Photobiol. C: Rev. 5 (2004) 225-246
21. Braslavsky S.E. Glossary of terms used in photochemistry 3rd edition. Pure Appl. Chem. 79 (2007) 293-465
22. Guzsvány V.J., Gaál F.F., Bjelica L.J., and Ökrész S.N. Voltammetric determination of imidacloprid and thiamethoxam. J. Serb. Chem. Soc. 70 (2005) 735-743
23. Gaál F.F., Guzsvány V.J., and Bjelica L.J. Determination of various insecticides and pharmaceuticals using differently modified glassy carbon electrodes. J. Serb. Chem. Soc. 72 (2007) 1465-1475
24. Bruccoleri A., Langford C.H., and Arbour C. Pulsed photo acoustic evaluation of intersystem crossing quantum yields in fulvic acid. Environ. Technol. Lett. 11 (1990) 169-172
25. Bruccoleri A., Pant B., Sharma D.K., and Langford C.H. Evaluation of primary photoproduct quantum yields in fulvic acids. Environ. Sci. Technol. 27 (1993) 889-894