Solvent and solvation effects on reactivities and mechanisms of phospho group transfers from phosphate and phosphinate esters to nucleophiles.

Organophosphorus esters fulfil many industrial, agricultural, and household roles. Nature has deployed phosphates and their related anhydrides as energy carriers and reservoirs, as constituents of genetic materials in the form of DNA and RNA, and as intermediates in key biochemical conversions. The transfer of the phosphoryl (PO3) group is thus a ubiquitous biological process that is involved in a variety of transformations at the cellular level such as bioenergy and signals transductions. Significant attention has been paid in the last seven decades to understanding the mechanisms of uncatalyzed (solution) chemistry of the phospho group transfer because of the notion that enzymes convert the dissociative transition state structures in the uncatalyzed reactions into associative ones in the biological processes. In this regard, it has also been proposed that the rate enhancements enacted by enzymes result from the desolvation of the ground state in the hydrophobic active site environments, although theoretical calculations seem to disagree with this position. As a result, some attention has been paid to the study of the effects of solvent change, from water to less polar solvents, in uncatalyzed phospho transfer reactions. Such changes have consequences on the stabilities of the ground and the transition states of reactions which affect reactivities and, sometimes, the mechanisms of reactions. This review seeks to collate and evaluate what is known about solvent effects in this domain, especially their effects on rates of reactions of different classes of organophosphorus esters. The outcome of this exercise shows that a systematized study of solvent effects needs to be undertaken to fully understand the physical organic chemistry of the transfer of phosphates and related molecules from aqueous to substantially hydrophobic environments, since significant knowledge gaps exist.

Comparative adsorptive behaviour of cow dung ash and starch as potential eco-friendly matrices for controlled organophosphorus pesticides delivery.

The work reported herein explores the viability of cow dung ash (CDA) as a matrix for controlled pesticide delivery, by comparing its adsorptive characteristics towards two organophosphorus pesticides with those of starch, conventionally utilized in designing controlled pesticide delivery systems. CDA was characterized by Fourier transform infrared (FTIR) spectroscopy and powder X-ray diffraction (PXRD). Data for pesticide adsorption on the surfaces correlate well with Langmuir and Freundlich isotherms, with the former isotherm giving a slightly better fit (R2 ≥ 0.90) than the latter (R2 ≥ 0.81). Values of the adsorption parameters KL and RL indicate favourable pesticide adsorption on both surfaces. Desorption is the microscopic reverse of adsorption; both processes obey pseudo-second-order kinetics. The implication of this kinetic form is a mechanism in which adsorbate diffusion to the polymer surface and its transport into the polymer interior are important events. The isothermal and kinetic ratios, [Formula: see text] and 4.0, [Formula: see text] and 0.6, and [Formula: see text] and 1.0 at pH 7.0 and 27 °C, compare the adsorptive behaviour of diazinon and dichlorvos, respectively, on CDA and starch. These parameters are of the same order of magnitude, signalling that CDA is as potentially viable as starch for use as a matrix for pesticide-controlled delivery.

Reactions of aryl dimethylphosphinothioate esters with anionic oxygen nucleophiles: transition state structure in 70% water-30% ethanol.

Aryl dimethylphosphinates, 2, react with anionic oxygen nucleophiles in water via a concerted (ANDN) mechanism. With EtO- in anhydrous ethanol, the mechanism is associative (AN + DN), with rate-limiting pentacoordinate intermediate formation. This change in mechanism with solvent change has been ascribed to changes in the nucleophile and leaving group basicities accompanying solvent change. This paper reports on a kinetic analysis of the reactions of the aryl dimethylphosphinothioates, 3a-g, with oxygen nucleophiles in 70% water-30% ethanol (v/v) solvent at 25 °C, reactions known to proceed by a concerted mechanism in water, to test the rationalization stated above, since the nucleophiles and LGs of interest are more basic in aqueous ethanol than in water. The change in solvent causes an ca. 14 to 320-fold decrease in rate. Hammett and Brønsted-type correlations characterize a concerted TS with less P-LG bonding in aqueous ethanol than in water. Two opposing consequences are associated with the solvent change: (a) increased basicity of nucleophiles and LGs, which lead to a modest tightening of the TS; and (b) better stabilization of the IS relative to the TS in aqueous ethanol, which results in a slower reaction with a more product-like TS. Hammond and anti-Hammond effects on the TS arising from better stabilization of the IS over the TS dominate over the effects of increased nucleophile and LG basicity in determining the looser TS structure in aqueous ethanol. An altered TS structure is consistent with an altered reaction potential energy surface, in this case caused by a change in solvent polarity.

Ketonization of the remarkably strongly acidic elongated enol generated by flash photolytic decarboxylation of p-benzoylphenylacetic acid in aqueous solution.

Photodecarboxylation of p-benzoylphenylacetic acid in aqueous solution produces the elongated enol 5, whose strength as an oxygen acid (pQ(E/a)= 7.67) makes it more acidic than simple enol analogs by several orders of magnitude.

A concerted mechanism for the transfer of the thiophosphinoyl group from aryl dimethylphosphinothioate esters to oxyanionic nucleophiles in aqueous solution.

Earlier work on the hydrolysis of aryl phosphinothioate esters has led to contradictory mechanistic conclusions. To resolve this mechanistic ambiguity, we have measured linear free energy relationships (beta(nuc) and beta(lg)) and kinetic isotope effects for the reactions of oxyanions with aryl dimethylphosphinothioates. For the attack of nucleophiles on 4-nitrophenyl dimethylphosphinothioate, beta(nuc) = 0.47 +/- 0.05 for phenoxide nucleophiles (pK(a) < 11) and beta(nuc) = 0.08 +/- 0.01 for hydroxide and alkoxide nucleophiles (pK(a) >or= 11). Linearity of the plot in the range that straddles the pK(a) of the leaving group (4-nitrophenoxide, pK(a) 7.14) is indicative of a concerted mechanism. The much lower value of beta(nuc) for the more basic nucleophiles reveals the importance of a desolvation step prior to rate-limiting nucleophilic attack. The reactions of a series of substituted aryl dimethylphosphinothioate esters give the same value of beta(lg) with the nucleophiles HO(-) (beta= -0.54 +/- 0.03) and PhO(-) (beta = -0.52 +/- 0.09). A significantly better Hammett correlation is obtained with sigma(-) than with sigma or sigma degrees , as expected for a transition state involving rate-limiting cleavage of the P-OAr bond. The (18)O KIE at the position of bond fission ((18)k = 1.0124 +/- 0.0008) indicates the P-O bond is approximately 40% broken, and the (15)N KIE in the leaving group ((15)k = 1.0009 +/- 0.0003) reveals the nucleofuge carries about a third of a negative charge in the transition state. Thus, both the LFER and KIE data are consistent with a concerted reaction and disfavor a stepwise mechanism.

Catalysis of the ethanolysis of aryl methyl phenyl phosphinate esters by alkali metal ions: transition state structures for uncatalyzed and metal ion-catalyzed reactions.

This paper reports on a spectrophotometric kinetic study of the effects of the alkali metal ions Li+ and K+ on the ethanolysis of the aryl methyl phenyl phosphinate esters 3a-f in anhydrous ethanol at 25 degrees C. Rate data obtained in the absence and presence of complexing agents afford the second-order rate constants for the reaction of free ethoxide (k(EtO-)) and metal ion-ethoxide ion pairs (k(MOEt)). The sequence k(EtO-) < k(MOEt) is established for all the substrates, contrary to the generally observed reactivity order in nucleophilic substitution processes. The quantities deltaG(ip), deltaG(ts) and DeltaG(cat), which quantify the observed alkali metal ion effect in terms of transition state stabilization through chelation of the metal ion, give the order deltaG(ts) > deltaG(ip) for Li+ and K+. Hammett plots show significantly better correlation of rates with sigma and sigma(o) substituent constants than with sigma-, yielding moderately large rho(rho(o)) values that are consistent with a stepwise mechanism in which formation of a pentacoordinate (phosphorane) intermediate is the rate-limiting step. The range of the values of the selectivity parameter, rho(n) (= rho]/rho(eq)), 1.3-1.6, obtained for the uncatalyzed and alkali metal ion catalyzed reactions indicates that there is no significant perturbation of the transition state (TS) structure upon chelation of the metal ions. This finding is relevant to the mechanism of enzymatic phosphoryl transfer involving metal ion co-factors. The present results enable one to compare structural effects for nucleophilic reactions of several series of organophosphorus substrates. It is shown that the order of reactivity of the substrates: 4-nitrophenyl dimethyl phosphinate (2) > 3a > 4-nitrophenyl diphenyl phosphinate (1) is determined mainly by the steric effects of the alkyl/aryl substituents around the central P atom in the TS of the reaction.

Hydration of phenylketene revisited: a counter-intuitive result.

In previous work (Can. J. Chem. 1987, 65, 1719-1723 and J. Am. Chem. Soc. 1995, 117, 9165-9171), flash photolysis of diazoacetophenone or phenylhydroxycyclopropenone in aqueous solution was found to produce phenylketene as a short-lived transient species with absorbance at lambda congruent with 260 nm, which decayed with single-exponential kinetics. It has now been discovered that, in the acidity region [H(+)] = 0.000 01 to 0.06 M, this decay is preceded by a faster absorbance rise, and that the overall change conforms well to a double exponential rate law. Analysis of the new data produces rate profiles whose general shapes, as well as the numerical values of their constituent rate constants, plus the form of buffer catalysis, indicate that this newly discovered absorbance rise represents ketonization of phenylacetic acid enol, and that the subsequent absorbance decay represents addition of water to phenylketene. The chemistry of the system, however, requires ketene hydration to precede enol ketonization in a time sequence opposite from that of the absorbance changes. This seemingly counter-intuitive result is nevertheless consistent with the rate law that governs the time evolution of the central species in a two-step rise and decay, such as that observed here.

Nucleophilic displacement on 4-nitrophenyl dimethyl phosphinate by ethoxide ion: alkali metal ion catalysis and mechanism.

We report on a spectrophotometric kinetic study of the effect of Li(+) and K(+) cations on the ethanolysis of 4-nitrophenyl dimethylphosphinate () in ethanol at 25 [degree]C. The nucleophilic displacement reaction of with LiOEt and KOEt in the absence and presence of 18-crown-6 ether (18-C-6) furnished observed first-order rate constants which increase in the order EtO(-) < KOEt < LiOEt. The kinetic data are analyzed in terms of a scheme which assigns concurrent kinetic activity to free ethoxide and metal alkoxide, to obtain the second-order rate coefficients for reaction of the metal ion-ethoxide pairs, k(MOEt). Derived [small delta]G(ip), [small delta]G(ts) and [capital Delta]G(cat) values quantify ground state and transition state stabilization by the metal ions to give [small delta]G(ts) > [small delta]G(ip) for Li(+) and [small delta]G(ts)[similar][small delta]G(ip) for K(+). These results indicate moderate catalysis by Li(+), with manifesting lesser susceptibility to catalysis than other substrates previously studied. Second-order rate constants for the reaction of the aryl dimethylphosphinates with free EtO(-) were obtained from plots of log k(obs)vs. [KOEt], measured in the presence of excess 18-C-6. Hammett plots with [sigma] and [sigma][degree] substituent constants give significantly better correlation of rates than [sigma](-) and yield a moderately large [small rho]([small rho][degree]) value; this is interpreted in terms of a stepwise mechanism involving rate-limiting formation of a pentacoordinate intermediate. Comparison of the present results with those of Williams on the aqueous alkaline hydrolysis of Me(2)P(O)-OPhX and Ph(2)P(O)-OPhX esters, establishes the rationale for a change in mechanism in the more basic EtO(-)/EtOH nucleophile/solvent system by a stepwise mechanism instead of a concerted one in aqueous base. Structure-reactivity correlations following Jencks show that the change in mechanism is accounted for by cross interactions between the nucleophile and the leaving group in the transition state. The observed duality of mechanism is rationalized on the basis of the More O'Ferrall-Jencks diagram, as a spectrum of transition states covering a wide range of nucleophile and leaving group basicities.