References
1. Karl, D. M.
(2014). Microbially Transformation of Phosphorus in the Sea: New Views of an
Old Cycle. Annu. Rev. Marrine Sci. 6, 279-337.
2. Kolodiazhnyi,O.I.
(2021). Phosphorus Compounds of Natural Origin: Prebiotic, Stereochemistry,
Stereochemistry, Application, Symmetry,13, 889.
3. Deaegere, A. and
Karplus, M. (1992). Hydrolysis Rate Difference between Cyclic and Acyclic
phosphate ester: Solvation versus Strain. J. Am. Chem. Soc. 115, 5316-5317.
4. Katz, M. J., Moon,
S.Y., Mondlock, J. E., Beyzavi, M. H., Stephenson, C. J., Hupp, J. T and Farha,
O. K. (2015). Exploiting parameter space in MOFs: a 20 –fold enhancement of
phosphate –ester hydrolysis with UiO-66-NH2.Chem. Sci. 6, 2286-2291.
5. Cao, X., Mabrouki, M., Mello, S.V., Leblance, R. M.; Rastogi, V.
K.,Cheng, T.C., Defrank, J.J.(2005). The interaction between OPH and paraoxon
at the air –water interface studied by AFM and epifluorescence microscopies. J. Colloids & Surfaces. B: Biointerfaces, 40, 75.
6. Barrozo, A.,
Nelson, D. B., William, N. H. and Kamerlin, S. C. L. (2017). The effect of
magnesium ions on triphosphate
hydrolysis. Pure Apple. Chem. 89(6): 715- 727.
7. Saquib, Q.,
Al-Salem, A. M.,Siddiqui, M. A., Ansari, S. M.,Zhang,,X. and Al-Khedhairy, A.
A. (2022). Oranophosphorus Flame Retardant TDCPP Displays Genotoxic and
Carcinogenic Risks in Human Liver Cells. Cells, 11,195.
8.
Chen, M., Koekkoek, J. and Lamoree , M. (2022).
Organophosphate ester metabolites in human breast milk determined by online
solid phase extraction coupled to high pressure liquid chromatography tandem
mass spectrometry. Environment International,159, 107049.
9. Olivero-Verbel, R., Moreno,T., Fernández-Arribas, J.,
Reche.C., Minguillon, M. C., Martins, V., Querol, Q., Johnson-Restrepo, B., and
Eljarrat, E.(2021). Organophosphate esters in airborne particles from subway
stations. Science of the Total Environment. 769, 145105.
10. Ghosh, K. K. and
Patle, S. K. (2002). Kinetic solvent effects on reaction rates for the acidic hydrolysis
of dihydoxamic acid. 41A, 758-762.
11. Harifi-Mooda, A. R., Habibi-Yangjehb, A. and Gholamia, M. R.(2008).Kinetics study of a
Diels-Alder reaction in mixtures of an ionic liquid with molecular solvents. J.
Phys. Org. Chem. 21, 783–788.
12. Pross, A.(1995).Theoratical and Physical Principles of Organic
Reactivity. J Wiley & Sons. New York, Part B.
13. Riechardt, C.(1998). Solvents and Solvent Effects in organic
Chemistry, 2nd ed.; VCH; Winsheim
Germany.
14. Yadav, H. and
Bhoite, S. A. (2015), Stydy of Solvent Effects on the Acidic hydrolysis of Mono –n-ethyl-o-touidine Phosphate.Acta
Ciencia Indica, XL,(2) 67.
15. Chhetri, N. and
Bhoite, S. A. (2018). Micellar catalyzed hydrolysis of mono-2,3-dichloroaniline
phosphate. Journal of Dispersion Science and Technology. 39 (5), 644-654.
16. Allen, R.J.L.
(1940),The Estimation of Phosphorus.Biochem.J.34,858-865.
17. Ingold, C. K. and
Hughes, E. D. (1953). Stucture and Mechanism in Organic
Chemistry, Bell and sons, London, 310, (3),45.
18. Hughes, E.D.and Ingold, C.K. (1935).
Mechanism of substitution at a saturated carbon atom. PartIV. A discussion of
constitutional and solvent effect on the mechanism, kinetics, velocity and
orientation of substitution. J.Chem.Soc.
255.
19. Choure, N. and Bhoite, S.(2009).Kinetic study of
solvent effects on the hydrolysis of di-2-chloroaniline phosphate in dioxane
and dimethylnsulfoxide-water medium, J.Ind.Chem.Soc. 86,1335-1337.