1983
DOI: 10.1016/0097-8485(83)80004-7
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Test of Simonds′ method in factor analysis by digital simulation models

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Cited by 4 publications
(5 citation statements)
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“…Experimental studies usually rely on indirect methods like changes in NMR chemical shifts, UV or IR spectral changes, etc. However, difficulties derived from the failure of the analytical technique or of data treatment procedures have led in the past to a good deal of confusion and a spread of values for the protonation parameters of typical carbonyl compounds such as aromatic ketones, amides, , esters, and anilides, etc.…”
Section: Introductionmentioning
confidence: 99%
“…Experimental studies usually rely on indirect methods like changes in NMR chemical shifts, UV or IR spectral changes, etc. However, difficulties derived from the failure of the analytical technique or of data treatment procedures have led in the past to a good deal of confusion and a spread of values for the protonation parameters of typical carbonyl compounds such as aromatic ketones, amides, , esters, and anilides, etc.…”
Section: Introductionmentioning
confidence: 99%
“…This makes difficult to use them to identify acid catalyzed reactions, especially for reactions in which the solvated proton acts simultaneously as both the catalyst and reagent. The situation is saved by the following circumstance that is empirically observable: all scales of logarithmic acidity are practically linear in relation to one another, ie, Н о = β·Ноi . This should be reflected in practice because the macroreagent, ie, the acidic medium, should manifest itself in different ways on the micro level.…”
Section: Proton Aciditymentioning
confidence: 99%
“…Detailed overviews of the Н о values and acidity functions that are based on other indicators for various acidic systems are given in other works, the temperature dependence of Н о for sulfuric acid solutions has been studied in Gelbshtein et al and Liler, and the Н о of acid‐salt media and “mixed systems” (mixtures of mineral acids with solvents) are in previous studies . However, as it is justly stated in Uchnevich et al and Ostrovsky and Koldobsky, the introduction of a number of new acidity functions has not led to the establishment of a common view point; on the contrary, it introduced uncertainty into the concept of acidity.…”
Section: Proton Aciditymentioning
confidence: 99%
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