Revisiting the reactivity of oximate alpha-nucleophiles with electrophilic phosphorus centers. Relevance to detoxification of sarin, soman and DFP under mild conditions.

Following a potentiometric determination of the relevant pKa values of the (R1R2)C=NOH functionality, the second order rate constants (k(Ox)) for reaction of a large set of oximate bases with two model organophosphorus esters, i.e. bis-(4-nitrophenyl)phenylphosphonate (BNPPP) and bis-(4-nitrophenyl)methylphosphonate (BNPMP), and three toxic compounds, i.e., sarin (GB), soman (GD) and diisopropylphosphorofluoridate (DFP), in aqueous as well as a 30 : 70 (v/v) H2O-Me2SO mixture have been measured. The corresponding Brønsted-type nucleophilicity plots of log k(Ox)vs. pKa(Ox) reveal a clear tendency of the reactivity of the oximates to suffer a saturation effect with increasing basicity in aqueous solution. In the case of BNPMP and the three toxic esters, this behaviour is reflected in a levelling off at pKa approximately 9 but a more dramatic situation prevails in the BNPPP system where the attainment of maximum reactivity at pKa approximately 9 is followed by a clear decrease in rate at higher pKa's. Interestingly, a number of data reported previously by different authors for the sarin, soman and DFP systems are found to conform rather well to the curvilinear Brønsted correlations built with our data. Based on this and previous results obtained for reactions at carbon centers, it can be concluded that the observed saturation effect is the reflection of an intrinsic property of the oximate functionality. An explanation of this behavior in terms of an especially strong requirement for desolvation of the oximates prior to nucleophilic attack which becomes more and more difficult with increasing basicity is suggested. This proposal is supported by the observed changes in pKa(Ox) and k(Ox) brought about by a transfer from H2O to a 30 : 70 H2O-Me2SO mixture. The implications of the saturation effect on the efficiency of oximates as nucleophilic catalysts for smooth decontamination are emphasized. Also discussed is the effect of basicity on the exalted (alpha-effect) reactivity of these bases.

[1]  J. Epstein,et al.  The Chlorine-catalyzed Hydrolysis of Isopropyl Methylphosphonofluoridate (Sarin) in Aqueous Solution , 1956 .

[2]  Erwin Buncel,et al.  The α-effect and its modulation by solvent , 2004 .

[3]  C. F. Bernasconi The principle of imperfect synchronization: I. Ionization of carbon acids , 1985 .

[4]  M. Koupparis,et al.  Kinetic study and analytical applications of the micellar catalysed reactions of 1-fluoro-2,4-dinitrobenzene with thiols using a fluoride-selective electrode , 1993 .

[5]  G. Vanloon,et al.  Acceleration of nucleophilic attack on an organophosphorothioate neurotoxin, fenitrothion, by reactive counterion cationic micelles. Regioselectivity as a probe of substrate orientation within the micelle. , 2004, Langmuir : the ACS journal of surfaces and colloids.

[6]  R. Howd,et al.  Nonquaternary cholinesterase reactivators. 2. Alpha-heteroaromatic aldoximes and thiohydroximates as reactivators of ethyl methylphosphonyl-acetylcholinesterase in vitro. , 1984, Journal of medicinal chemistry.

[7]  I. Um,et al.  Effect of Solvent on the α-Effect: Nucleophilic Substitution Reactions of p-Nitrophenyl Acetate with m-Chlorophenoxide and Benzohydroxamates in MeCN−H2O Mixtures of Varying Compositions , 1997 .

[8]  G. Moutiers,et al.  Rapid Marcus Curvature Due to Extremely Strong Solvational Imbalances inthe Deprotonation of a Trinitrobenzylic Carbon Acid by Oximate Bases , 1999 .

[9]  C. F. Bernasconi,et al.  Ionization of Acetylacetone in Me2SO—Water Mixtures. Reactivity—Selectivity Principle or Principle of Imperfect Synchronization? , 1985 .

[10]  H. Michel,et al.  Charge effect in nucleophilic displacement reactions , 1967 .

[11]  A. J. Bennet,et al.  Catalytic recruitment by phosphonyl derivatives as inactivators of acetylcholinesterase and substrates for imidazole-catalyzed hydrolysis: .beta.-deuterium isotope effects , 1989 .

[12]  J. Halle,et al.  Utilisation des correlations de hammett a l'etude des equilibres tautomeres , 1972 .

[13]  S. Brant,et al.  Nonlinear Broensted correlations: The roles of resonance, solvation, and changing transition-state structure , 1982 .

[14]  G. Moutiers,et al.  Similar catalytic behaviour of oximate and phenoxide bases in theionization of bis(2,4-dinitrophenyl)methane in 50% water– 50%Me2SO. Revisiting the role of solvational imbalances indetermining the nucleophilic reactivity of α-effect oximate bases , 1997 .

[15]  E. Buncel,et al.  An AM1 study of an α-nucleophile: geometries and interconversion modes of oximate anion stereomers , 1989 .

[16]  Alan J. Parker,et al.  Protic-dipolar aprotic solvent effects on rates of bimolecular reactions , 1969 .

[17]  E. Buncel,et al.  Ground-State versus Transition-State Effects on the α-Effect as Expressed by Solvent Effects , 2001 .

[18]  J. Apostolakis,et al.  Use of ion-selective electrodes in kinetic flow injection: determination of phenolic and hydrazino drugs with 1-fluoro-2,4-dinitrobenzene using a fluoride-selective electrode. , 1991, The Analyst.

[19]  C. J. Murray,et al.  Nucleophilic addition to olefins. 18. Kinetics of the addition of primary amines and .alpha.-effect nucleophiles to benzylidene Meldrum's acid , 1986 .

[20]  C. F. Bernasconi Intrinsic barriers of reactions and the principle of nonperfect synchronization , 1987 .

[21]  E. Buncel,et al.  Physical Organic Chemistry of Reactions in Dimethyl Sulphoxide , 1977 .

[22]  M. L. Bender,et al.  REACTIONS OF GENERAL BASES AND NUCLEOPHILES WITH BIS(p-NITROPHENYL) METHYLPHOSPHONATE. , 1972 .

[23]  Ralph G. Pearson,et al.  The Factors Determining Nucleophilic Reactivities , 1962 .

[24]  R. Moss,et al.  Phosphorolytic reactivity of o-iodosylcarboxylates and related nucleophiles. , 2002, Chemical reviews.

[25]  G. Moutiers,et al.  The α-Effect in SNAr Substitutions − Reaction between Oximate Nucleophiles and 2,4-Dinitrofluorobenzene in Aqueous Solution , 2001 .

[26]  Shmaryahu Hoz,et al.  The α-Effect: A Critical Examination of the Phenomenon and Its Origin , 1985 .

[27]  Andrew Williams Concerted mechanisms of acyl group transfer reactions in solution , 1989 .

[28]  Jin Hong,et al.  The effect of solvent on the α-effect: CO, PO and SO2 centers , 2001 .

[29]  C. F. Bernasconi,et al.  INTRINSIC BARRIERS AND TRANSITION STATE STRUCTURES IN THE GAS PHASE CARBON-TO-CARBON IDENTITY PROTON TRANSFERS FROM NITROMETHANE TO NITROMETHIDE ANION AND FROM PROTONATED NITROMETHANE TO ACI-NITROMETHANE. AN AB INITIO STUDY , 1997 .

[30]  C. F. Bernasconi,et al.  Kinetics of ionization of 1,3-indandione in methyl sulfoxide-water mixtures. Solvent effect on intrinsic rates and Broensted coefficients , 1986 .

[31]  Robert B. Wilson,et al.  Base-catalyzed hydrolysis of 1,2,2-trimethylpropyl methylphosphonofluoridate—An examination of the saturation effect , 1988 .

[32]  Young-Min Park,et al.  The effect of solvent on the α-effect: the MeCN–H2O solvent system , 2000 .

[33]  K. R. Fountain,et al.  The alpha-Effect in Benzyl Transfers from Benzylphenylmethyl Sulfonium Salts to N-Methylbenzohydroxamate Anions. , 1999, The Journal of organic chemistry.

[34]  C. Broomfield,et al.  Unique push-pull mechanism of dealkylation in soman-inhibited cholinesterases. , 1997, Biochemistry.

[35]  D. Hupe,et al.  The effect of solvation on .beta. values for nucleophilic reactions , 1977 .

[36]  Y. Ashani,et al.  Nucleophilicity of heteroaromatic aldoximes bearing an aminoalkyl side chain. , 1970, Journal of medicinal chemistry.

[37]  E. Buncel,et al.  Reactions of oximate alpha-nucleophiles with esters: evidence from solvation effects for substantial decoupling of desolvation and bond formation. , 2002, Journal of the American Chemical Society.

[38]  M. Koupparis,et al.  Kinetic-potentiometric determination of amino acids based on monitoring their reaction with dinitrofluorobenzene using a fluoride-selective electrode. , 1987, The Analyst.

[39]  C. F. Bernasconi,et al.  Kinetics of Proton Transfer from 2-Nitro-4-X-phenylacetonitriles to Piperidine and Morpholine in Aqueous Me2SO. Solvent and Substituent Effects on Intrinsic Rate Constants. Transition State Imbalances , 1996 .

[40]  F. Raushel,et al.  Enhanced degradation of chemical warfare agents through molecular engineering of the phosphotriesterase active site. , 2003, Journal of the American Chemical Society.

[41]  F. G. Bordwell,et al.  Equilibrium Acidities in Dimethyl Sulfoxide Solution , 1988 .

[42]  P. Haake,et al.  A one-step synthesis of epoxyphosphonates , 1976 .

[43]  V. Veselov,et al.  The α-Effect in the Chemistry of Organic Compounds , 1978 .

[44]  Qinjian Zhao,et al.  Nucleophilic and protolytic catalysis of phosphonate hydrolysis : isotope effects and activation parameters , 1993 .

[45]  G. Wagner,et al.  Rapid Nucleophilic/Oxidative Decontamination of Chemical Warfare Agents , 2002 .

[46]  John O. Edwards,et al.  The alpha effect. A review , 1973 .

[47]  K. Ghosh,et al.  Nucleophilic dephosphorylation of p-nitrophenyl diphenyl phosphate in cationic micellar media. , 2005, Langmuir : the ACS journal of surfaces and colloids.

[48]  J. Speakman 164. The determination of the thermodynamic dissociation constants of dibasic acids , 1940 .

[49]  G. Moutiers,et al.  The levelling effect of solvational imbalances in the reactions of oximate alpha-nucleophiles with electrophilic phosphorus centers. Relevance to detoxification of organophosphorus esters. , 2003, Chemical communications.

[50]  C. E. Efstathiou,et al.  Semi-automated kinetic determination of phenolic compounds using a fluoride-selective electrode and based on their micellar-catalysed reaction with 1-fluoro-2,4-dinitrobenzene , 1989 .

[51]  F. Terrier,et al.  Sulfur derivatives of 2-oxopropanal oxime as reactivators of organophosphate-inhibited acetylcholinesterase in vitro: synthesis and structure-reactivity relationships. , 1988, Journal of Medicinal Chemistry.

[52]  Um,et al.  The origin of the alpha-effect: dissection of ground-state and transition-state contributions , 2000, The Journal of organic chemistry.

[53]  M. Koupparis,et al.  Kinetic determination of primary and secondary amines using a fluoride-selective electrode and based on their reaction with 1-fluoro-2,4-dinitrobenzene , 1989 .

[54]  A. Hengge,et al.  A concerted mechanism for the transfer of the thiophosphinoyl group from aryl dimethylphosphinothioate esters to oxyanionic nucleophiles in aqueous solution. , 2005, Journal of the American Chemical Society.

[55]  W. Jencks,et al.  Nonlinear structure-reactivity correlations. Acyl transfer between sulfur and oxygen nucleophiles , 1977 .

[56]  K. Patel,et al.  Evidence That the α-Effects in Methyl Transfers from Aryldimethylsulfonium Salts Correlate with Single-Electron-Transfer Characteristics , 1997 .

[57]  A. Martell,et al.  A Kinetic Study of the Copper(II) Chelate Catalyzed Hydrolysis of Diisopropyl Phosphorofluoridate , 1963 .

[58]  James A. Baker,et al.  Decontamination of chemical warfare agents , 1992 .

[59]  F. Mancin,et al.  Activation of oximic nucleophiles by coordination of transition metal ions , 2000 .

[60]  M. Koupparis,et al.  Kinetic study and analytical applications of micellar catalyzed reactions of 1-fluoro-2,4-dinitrobenzene with inorganic thioanions using a fluoride-selective electrode. , 2000, Talanta.

[61]  A. L. Green,et al.  756. The reaction of oximes with isopropyl methylphosphono-fluoridate (Sarin) , 1956 .

[62]  D. Herschlag,et al.  Decreasing reactivity with increasing nucleophile basicity. The effect of solvation on .beta.nuc for phosphoryl transfer to amines. , 1986, Journal of the American Chemical Society.

[63]  L. Debussche,et al.  Polymethylenedioxy bis(2-hydroxyiminomethylpyridinium) as in vitro reactivators of organophosphorous inhibited eel acetylcholinesterase , 1988 .

[64]  R. Howd,et al.  Structure-activity relationships for reactivators of organophosphorus-inhibited acetylcholinesterase: quaternary salts of 2-[(hydroxyimino)methyl]imidazole. , 1984, Journal of medicinal chemistry.

[65]  Andrew Williams,et al.  Effective Charge and Transition-state Structure in Solution , 1992 .

[66]  A. Martell,et al.  A Kinetic Study of the Copper(II) Chelate-catalyzed Hydrolysis of Isopropyl Methylphosphonofluoridate (Sarin) , 1962 .

[67]  H. Benschop,et al.  Nerve agent stereoisomers: analysis, isolation and toxicology , 1988 .

[68]  Erwin Buncel,et al.  Origin of the Bell-Shaped .alpha.-Effect-Solvent Composition Plots. pKa-Solvent Dependence of the .alpha.-Effect at a Phosphorus Center , 1995 .

[69]  P. Gosselin,et al.  Enhanced reactivity of an α-nucleophile in water-dimethyl sulfoxide mixtures. A transition state effect. , 1984 .

[70]  D. Herschlag,et al.  Nucleophiles of high reactivity in phosphoryl transfer reactions: .alpha.-effect compounds and fluoride ion , 1990 .

[71]  P. Eyer,et al.  Kinetic analysis of interactions between human acetylcholinesterase, structurally different organophosphorus compounds and oximes. , 2004, Biochemical pharmacology.

[72]  Y. Ashani,et al.  Nucleophilicity of some reactivators of phosphorylated acetylcholinesterase. , 1971, Journal of medicinal chemistry.

[73]  G. Moutiers,et al.  Use of a Fluoride Ion Selective Electrode as a Tool for Monitoring Relatively Fast Kinetic Processes. Applications to the Hydrolysis of Organofluorophosphorus Esters and 2,4‐Dinitrofluorobenzene , 2000 .

[74]  C. Lion,et al.  Non-linear Brønsted correlations: evidence for a levelling off in the reactivity of oximate ions in aqueous solution , 1991 .

[75]  C. F. Bernasconi The Principle of Non-perfect Synchronization , 1992 .