1939
DOI: 10.1039/jr9390000920
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Cited by 13 publications
(17 citation statements)
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“…The molar absorptivities of 1 and I1 were calculated a t each absorption maximum as well as a t each distinct vibrational band and agreed with published values (31,32). The molar absorptivities of the bound mono-cation& of I and I1 were calculated from the absorbances of solutions of the probes in which pH = pKa -2 and to which a sufficient excess of DNA was added so that further addition of DNA produced no perceptible changes in the absorption.…”
Section: ) Of the Compoundssupporting
confidence: 68%
“…The molar absorptivities of 1 and I1 were calculated a t each absorption maximum as well as a t each distinct vibrational band and agreed with published values (31,32). The molar absorptivities of the bound mono-cation& of I and I1 were calculated from the absorbances of solutions of the probes in which pH = pKa -2 and to which a sufficient excess of DNA was added so that further addition of DNA produced no perceptible changes in the absorption.…”
Section: ) Of the Compoundssupporting
confidence: 68%
“…The reliability and consistency of the results can be evaluated by using the consistency standard deviation, which is defined by Equation (6). (6) During this work the total number of measurements (n m ) carried out to determine the pK a values was 86 for a total number of compounds (n c ) of 30, hence the consistency parameter s = 0.04, which indicates good consistency of the data.…”
Section: Resultsmentioning
confidence: 99%
“…The commonly cited, directly measurable experimental value for the aqueous pK a of quinazoline (pK a = 3.51 [6] ) actually corresponds to a more complex equilibrium involving the covalent hydration of quinazoline. [29] A correct experimentally measured aqueous pK a corresponding to the pK a defined in Equation (1) is 1.95.…”
Section: Quinazolinementioning
confidence: 99%
See 1 more Smart Citation
“…Pyridine 110-86-1 5.23 [79] 3.4 [60] 12.53 [33] [e] 5.5 [63] 214.7 2,2′-Bipyridine 366-18-7 4.23 [80] 12.27 [36] [e] 223.1 Quinoline 91-22-5 4.93 [79] 11.97 [36] [e] 220.2 2,2′-Biquinoline 119-91-5 3.66 [67] 11.28 [36] [e] 230.0 [36] [g] Isoquinoline 119-65-3 5.46 [79] 12.68 [36] [e] 219.9 Acridine 260-94-6 5.62 [79] 12.66 [36] [e] 224.8 Phenanthroline 66-71-7 5.12 [81] 13.69 [36] [e] 230.9 [36] [g] Imidazole 288-32-4 6.95 [82] 6.26 [83] 15.07 [36] [e] 9.4 ± 1.8 [d] 217.3 Benzimidazole 51-17-2 5.56 [84] 4.36 [83] 13.54 [36] [e] 220.0 1,2,3-Triazole 288-36-8 1.17 [85] 0.0 ± 1.2 [d] 8.0 [36] [e] 2.5 ± 1.8 [d] 202.5 Benzotriazole 95-14-7 0.42 [86] 6.89 [36] [e] 210.2 [36] [g] Pyrazole 288-13-1 2.48 [85] 1.0 ± 1. [87] 7.61 [36] [e] 207.7 Pyridazine 289-80-5 2.33 [79] 1.8 ± 1.2 [d] 10.06 [36] [e] 3.7 ± 1.8 [d] 209.6 Pyrimidine 289-95-2 1.3 [79] 0.55 [88] 8.72 [36] [e] 2.4 ± 1.8 [d] 204.5 Pyrazine 290-37-9 0.6 [79] -0.2 ± 1.2 [d] 7.74…”
Section: Cyclic Aminesmentioning
confidence: 99%