2017
DOI: 10.1016/j.jpba.2017.05.038
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Proton dissociation properties of arylphosphonates: Determination of accurate Hammett equation parameters

Abstract: Determination of the proton dissociation constants of several arylphosphonic acid derivatives was carried out to investigate the accuracy of the Hammett equations available for this family of compounds. For the measurement of the pK values modern, accurate methods, such as the differential potentiometric titration and NMR-pH titration were used. We found our results significantly different from the pK values reported before (pK: MAE = 0.16 pK: MAE=0.59). Based on our recently measured pK values, refined Hammet… Show more

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Cited by 9 publications
(10 citation statements)
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“…S2 †. The initial shift to lower ppm over time is consistent with initial aggregation of the linker (as per the control experiments just described and in agreement with conclusions from the SAXS experiments described below), but is also consistent with the direction of anticipated peak shifts on deprotonation of the BTPPA phosphonic acid groups, 41–44 most notably observed in H c at the ortho position with respect to the phosphonic acid substituents. 41,45–47 Subsequent to these two combined effects, and on a more rapid timescale with increasing temperature, a marked swing in the other direction downfield to higher ppm is observed for all the aromatic protons, in line with metal coordination counteracting and exceeding the effects of deprotonation in particular.…”
Section: Resultssupporting
confidence: 86%
“…S2 †. The initial shift to lower ppm over time is consistent with initial aggregation of the linker (as per the control experiments just described and in agreement with conclusions from the SAXS experiments described below), but is also consistent with the direction of anticipated peak shifts on deprotonation of the BTPPA phosphonic acid groups, 41–44 most notably observed in H c at the ortho position with respect to the phosphonic acid substituents. 41,45–47 Subsequent to these two combined effects, and on a more rapid timescale with increasing temperature, a marked swing in the other direction downfield to higher ppm is observed for all the aromatic protons, in line with metal coordination counteracting and exceeding the effects of deprotonation in particular.…”
Section: Resultssupporting
confidence: 86%
“…This allows a quantitative description of the molecule by showing the influence of the substituents. For aromatic rings with more than one substituent, the additive nature of the σ coefficients can be assumed (with some caution) [29,30]. The substituent constants found in the literature are presented in Table 3 [31,32].…”
Section: The Hammett Constantmentioning
confidence: 99%
“…Arylphosphonates are the products of another approach comprising the MW‐assisted catalytic Arbuzov reaction of aryl bromides with triethyl phosphite. In the presence of a Ni salt catalyst, the phosphonates could be prepared in yields of 67–86 % ,. The MW irradiation “overcame” the decreased reactivity of aryl bromides (Scheme ).…”
Section: The Substitution or Simplification Of Catalyst Systems By/unmentioning
confidence: 99%