Chemometric Analysis of Substituent Effects. X. Unification and Reparametrization of Substituent Constants in Hammett-Type Equations by Means of Alternative Interpretation of Substituent Effects (AISE)

1996 ◽  
Vol 61 (8) ◽  
pp. 1191-1204 ◽  
Author(s):  
Oldřich Pytela
Keyword(s):  
Standard Deviation ◽  
Substituent Effects ◽  
Alternative Interpretation ◽  
The Other ◽  
Substituent Constant ◽  
Residual Standard Deviation ◽  
Regression Parameters ◽  
Substituent Constants ◽  
Predicted Values ◽  
A Current

The paper deals with evaluation of validity of substituent scales σm, σp, σp0, σp+, and σp- in Hammett-type equations. Possible reasons of unreliability of these scales and conceivable ways of verification of individual substituent constants are discussed. On the basis of Alternative Interpretation of Substituent Effects (AISE) and four additional conditions, a regression nonlinear model has been suggested which includes the dependence of all above-mentioned substituent scales upon a single interpreting variable - the σi substituent constant. This model has been applied to the 32 most frequent substituents from each scale, i.e. altogether 160 substituent constants taken from literature. The optimization of 17 unknown regression parameters gave the residual standard deviation s = 0.180 and, after excluding 12 remote values, s = 0.061. The analysis of residua proved their standard and statistical appropriateness of the model. The agreement between literature values and predicted values of substituent constants was the best with the σm scale; on the other hand, the largest differences were encountered with the σp+ scale. The found differences above a current reliability limit of substituent constants were due first to unreliability of some literature data and next to solvent effects and (in some cases) specific properties of substituents.

Chemometric Analysis of Substituent Effects. VIII. Alternative Interpretation of Substituent Effects (AISE)

1995 ◽  
Vol 60 (9) ◽  
pp. 1502-1528 ◽  
Author(s):  
Oldřich Pytela
Keyword(s):  
Multiple Bond ◽  
Substituent Effects ◽  
Alternative Interpretation ◽  
Class I ◽  
Reaction Centre ◽  
Correlation Equations ◽  
Class Iii ◽  
Substituent Constant ◽  
Chemical Models ◽  
The Individual

Alternative interpretation of substituent effects (AISE) starts from the presumption that a substituent only possesses a single property described by a single substituent constant. This property is transmitted to the reaction centre by three different ways depending on the interaction type in the triad reaction centre - basic skeleton - substituent. For interpretation it is substantial whether or not the substituent has p electrons at the atom adjacent to the basic skeleton. If it has none, the substituent belongs to class I and operates only by its basic effect described by the mentioned single substituent constant. Substituents of class II possess a free electron pair at the atom adjacent to the basic skeleton, and those of class III have a multiple bond between the first and the second atoms which is polarized in the direction from the basic skeleton. Substituent effects in class I are described by a substituent constant identical with σI constant. Substituents in classes II and III show additional effects proportional to the same constant. Hence, a separate treatment of substituent effects in the individual classes provides three straight lines intersecting in a common point. Mathematically, the description of substituent effects in this approach is expressed by a family of lines with a single explaining variable. The point of intersection, which is referred to as the iso-effect point, is not identical with the classic standard substituent - hydrogen - but is near to CN substituent. The approach given has the advantage of adopting a single substituent constant whose scale can be adjusted relatively precisely. Its drawback (like in the case of the correlation equations derived from the principle of separation of substituent effects) lies in a more extensive set of substituents needed for a correlation. The AISE principle has been applied to 318 series of experimental data describing effects of 32 substituents in a large variety of chemical models (aliphatic, alicyclic, aromatic, heteroaromatic, with or without direct conjugation between reaction centre and substituent) in both chemical reactions and equilibria. A comparison with two other correlation relations with two and three substituent constants for interpretation of substituent effects based on the principle of separation of the individual substituent effects showed that the closeness of AISE based correlations is comparable with that of the correlation equations currently used. It was somewhat less successful in the models with direct conjugation between reaction centre and substituent but the AISE principle can be used even in these cases.

Substituent Effects on the Acetyl Group Conformation and the Carbonyl Frequency in Acetophenones

1973 ◽  
Vol 51 (9) ◽  
pp. 1363-1367 ◽  
Author(s):  
P. J. Krueger
Keyword(s):  
Standard Deviation ◽  
Correlation Coefficient ◽  
Resonance Effect ◽  
Substituent Effects ◽  
Intramolecular Hydrogen Bonding ◽  
Carbonyl Groups ◽  
Dipole Interactions ◽  
Acetyl Group ◽  
Substituent Constants ◽  
Intramolecular Hydrogen

The fundamental carbonyl stretching frequencies for o-, m-, and p-substituted acetophenones in dilute CCl4 solution are correlated with the electrophilic substituent constant σ+ by the expression vc=o (cm−1) = 11.53σ+ + 1691.5 (n = 27, correlation coefficient = 0.988, standard deviation = 1.2 cm−1). The frequencies of carbonyl groups trans to an o-substituent follow this correlation, assuming σo+ ≈ σp+, while those oriented cis to the substituent generally do not. Deviations from this correlation are interpreted in terms of dipole–dipole interactions, steric hindrance to planarity, intramolecular hydrogen bonding, and non-additivity of σ+ values for some combinations of substituents. The carbonyl frequencies for singly m- and p-substituted acetophenones are also correlated with the polar and resonance components of σ+ by the expression vc=o (cm−1) = 15.66σI + 10.99σR+ + 1689.8 (n = 13, correlation coefficient = 0.981, standard deviation = 0.9 cm−1). Thus the sensitivity of the carbonyl frequency to the polar effect is greater than to the resonance effect. In ω-substituted acetophenones no precise correlation with polar substituent constants is observed.

Multinuclear (1H, 13C and 15N) Magnetic Resonance Spectroscopy and Substituent Effects on N-Phenoxyethylanilines

2002 ◽  
Vol 57 (2) ◽  
pp. 226-232 ◽  
Author(s):  
Jorge L. Jios ◽  
Gustavo P. Romanelli ◽  
Juan C. Autino ◽  
Damian Magiera ◽  
Helmut Duddeck
Keyword(s):  
Magnetic Resonance ◽  
Magnetic Resonance Spectroscopy ◽  
Substituent Effect ◽  
Nmr Spectra ◽  
Chemical Shifts ◽  
Substituent Effects ◽  
The Other ◽  
Resonance Spectroscopy ◽  
Phenyl Rings ◽  
Substituent Constants

1H, 13C and 15N NMR spectra of twenty substituted N-phenoxyethylanilines 1-20 were completely and unambiguously assigned using a combination of both homo- and heteronuclear (gs-COSY), 1H detected heteronuclear one-bond (gs-HMQC) and long-range (gs- HMBC) gradient-selected correlation experiments. Correlations between chemical shifts and substituent constants are analyzed separately for both phenyl rings using variable substituents para to the fixed substituent -OCH2CH2NHC6H5 (series I) and -NHCH2CH2OC6H5 (series II), respectively. The correlation coefficient for chemical shifts vs. a linear combination of inductive and resonance substituent constants is high and improves when only the six values, corresponding to each para-monosubstituted series, were used. For nitrogen chemical shifts excellent linear dependences were obtained. The results show that the ethylene chain is not able to transmit the substituent effect from one aromatic ring to the other.

Chemometrical analysis of substituent effects on 13C and 15N NMR chemical shifts in 1-aroyl-3-substituted thioureas

1989 ◽  
Vol 54 (9) ◽  
pp. 2399-2407 ◽  
Author(s):  
Oldřich Pytela ◽  
Josef Jirman ◽  
Antonín Lyčka
Keyword(s):  
Latent Variables ◽  
Chemical Shifts ◽  
Substituent Effects ◽  
The Other ◽  
15N Nmr ◽  
Nmr Chemical Shifts ◽  
Additional Constant ◽  
Substituent Constants ◽  
Derivatives Of ◽  
C Nmr

The methods of conjugated deviations and regression analysis have been used to study the substituent effects on 13C and 15N NMR chemical shifts of 12 derivatives of 1-aroyl-3-phenylthiourea and 1-aroyl-3-methylthiourea. The 13C NMR chemical shifts can be described by two latent variables, one univocally correlated with the Hammett substituent constants (r = 0.993) and the other reflecting the increased shielding of the nuclei due to overlap of the adjacent bond electrons as a consequence of electron-donor or electron-acceptor character of the substituents.This effect is less pronounced with the 15N nuclei. Application of dual substituent constants σR, σF with the additional constant σα describing the polarization has failed in giving sufficiently close correlations and explanation of the substituent effect found.

Chemometric Analysis of Substituent Effects. II. Relation Between Hammett Substituent Constants σm and σp and a New Model for Quantitative Description of Substituent Effects

1994 ◽  
Vol 59 (2) ◽  
pp. 381-390 ◽  
Author(s):  
Oldřich Pytela
Keyword(s):  
Dissociation Constants ◽  
General Relation ◽  
Quantitative Description ◽  
Substituent Effects ◽  
Data Series ◽  
Reaction Centre ◽  
Substituent Constant ◽  
New Model ◽  
Resonance Effects ◽  
Substituent Constants

The paper presents values of 25 substituent constants σi obtained by optimizing 46 data series of dissociation constants of substituted benzoic acids in various media. The constants σi fulfil the general relation between the substituent constants of the Hammett type in meta and para positions enabling the description of substituent effects from both positions at the same time by a single constant. The Hammett substituent constants are interpreted by means of the σi constants with an accuracy better than 0.03 units. In addition to it, the validity of general relationship between σp and σm was verified on a set of 56 substituents with the prediction accuracy of 0.06 units for σp, and after excluding the probably incorrectly parametrized substituents NHCOC6H5, CH3S, and F the accuracy has improved to 0.05 units (98% of interpreted variability). The given relationship has served as a basis for suggesting a new model of transfer of substituent effects to a reaction centre: the model involves both the Hammett equation and the Yukawa-Tsuno equation and explains their background. The suggested model uses generalized transmission coefficients to separately describe the transformation of a single primary substituent effect - depending on its structure - into one inductive and two resonance effects which are transmitted through two independent channels to the reaction centre and here transformed into the resulting observable effect. From the model it follows that the substituent constant σp is not a substituent constant in the true sense of the word since it involves the characteristics of skeleton and of reaction centre.

Chemometrical Analysis of Substituent Effects. V. ortho Effect

1994 ◽  
Vol 59 (9) ◽  
pp. 2005-2021 ◽  
Author(s):  
Oldřich Pytela ◽  
Josef Liška
Keyword(s):  
Dissociation Constants ◽  
Substituent Effects ◽  
Reaction Centre ◽  
Benzoic Acids ◽  
Electronic Effects ◽  
Substituent Constant ◽  
Zero Values ◽  
Substituent Constants ◽  
Substituted Benzoic Acids ◽  
Intramolecular Hydrogen

The dissociation constants of nineteen ortho substituted benzoic acids have been determined in eight organic solvents (methanol, ethanol, acetone, dimethyl sulfoxide, dimethylformamide, acetonitrile, pyridine, 1,2-dichloroethane). The correlation between the σI, σR, and υ constants were unsuccessful due to neglecting the description of intramolecular hydrogen bond effect. The method of conjugated deviations has been applied to the results obtained and to those given in literature for ortho substituted benzoic acids (the dissociation constants, the reaction with diphenyldiazomethane, 33 sets), and values of three types of substituent constants have been determined for 29 substituents. The first of these substituent constants, σoi, describes the electronic effects and was adjusted with the application of the isoparameter relation (σoi as a function of σmi) suggested in previous communications. This constant (after excluding the substituents NHCOCH3 and OCOCH3) correlates very well (R = 0.993) with the σI and σR constants. The second substituent constant, σHGi, describes the interaction of the reaction centre (the oxygen atom of carboxylate anion) with the substituent, and it has non-zero values for the substituents OH, SH, NH2, NHCH3, NHCOCH3, COOH, CONH2, and SO2NH2. The third substituent constant, σSi, describes the steric effects and is not significantly related to any of the known quantities of this type. The set given was tested together with the triad of σI, σR, and υ on the definition set and on a set extended by other 28 sets of processes with ortho substituted compounds. On the whole, the set of substituent constants suggested explains 94.6% of variability of data, whereas only 66.0% are explained with the use of σI, σR, and u constants. Moreover, the tests have shown that the σoi constant is not suitable for interpretations of processes involving direct conjugation between the reaction centre and substituent.

Substituent effects on selectivity of coupled oxidation of iron tetraphenylporphyrins

2015 ◽  
Vol 19 (05) ◽  
pp. 726-733 ◽  
Author(s):  
Kazuhisa Kakeya ◽  
Atsuko Shimizu ◽  
Kenta Akasaka ◽  
Tadashi Mizutani
Keyword(s):  
Nitro Group ◽  
Oxidation Rate ◽  
Substituent Effects ◽  
Para Position ◽  
Positive Slope ◽  
Substituent Constant ◽  
Meso Position ◽  
Substituent Constants

Coupled oxidation of iron tetraphenylporphyrins bearing either a OMe , Me , F , Cl , COOMe , CF 3 or CN group in the para-position of the phenyl groups gave tetraarylbiladien-ab-1-one and triarylbilindione. The ratios of the yields of the former to those of the latter were linearly correlated with the Hammett substituent constants σp+, with a positive slope (Δρ = 0.64). The Hammett plot of the oxidation rate vs. the substituent constant σp also showed a positive slope (ρ = 0.30). These substituent effects suggest that a nucleophilic step is included in the formation of bilindione. Coupled oxidation of an A3B type tetraarylporphyrin having an electron withdrawing nitro group in one of the phenyl groups indicated that the oxidation leading to biladienone occurred rather statistically in any of the meso-positions, while the oxidation leading to bilindione occurred preferentially in the meso-position bearing the 4-nitrophenyl group.

Rem Study of Current Effect on the Structure of Clean Si(111) Surface

1990 ◽  
Vol 48 (1) ◽  
pp. 306-307
Author(s):  
A. Yamanaka ◽  
H. Ohse ◽  
K. Yagi
Keyword(s):  
The Other ◽  
Current Direction ◽  
Clean Surface ◽  
Current Effect ◽  
Atomic Steps ◽  
Step Bunching ◽  
Terrace Width ◽  
Step Down ◽  
A Current

Recently current effects on clean and metal adsorbate surfaces have attracted much attention not only because of interesting phenomena but also because of practically importance in treatingclean and metal adsorbate surfaces [1-6]. In the former case, metals deposited migrate on the deposit depending on the current direction and a patch of the deposit expands on the clean surface [1]. The migration is closely related to the adsorbate structures and substrate structures including their anisotropy [2,7]. In the latter case, configurations of surface atomic steps depends on the current direction. In the case of Si(001) surface equally spaced array of monatom high steps along the [110] direction produces the 2x1 and 1x2 terraces. However, a relative terrace width of the two domain depends on the current direction; a step-up current widen terraces on which dimers are parallel to the current, while a step-down current widen the other terraces [3]. On (111) surface, a step-down current produces step bunching at temperatures between 1250-1350°C, while a step-up current produces step bunching at temperatures between 1050-1250°C [5].In the present paper, our REM observations on a current induced step bunching, started independently, are described.Our results are summarized as follows.(1) Above around 1000°C a step-up current induces step bunching. The phenomenon reverses around 1200 C; a step-down current induces step bunching. The observations agree with the previous reports [5].

Substituent effects in 1,3-indanediones

1982 ◽  
Vol 47 (5) ◽  
pp. 1486-1493 ◽  
Author(s):  
Alexander Perjéssy
Keyword(s):  
Substituent Effects ◽  
Empirical Equations ◽  
Substituent Constants ◽  
Complex Structural

The carbonyl stretching frequencies correlate well with substituent constants in a series of 166 1,3-indanediones using improved and extended Seth-Paul-Van Duyse equation. Transmissive factors and group electronegativities have been used to find empirical equations for calculation of substituent constants of more complex structural fragments.

Chemometric Analysis of Substituent Effects. VII. Inductive Effect as a Basic Substituent Effect. Isoeffect Substituent Constant

1995 ◽  
Vol 60 (8) ◽  
pp. 1316-1332 ◽  
Author(s):  
Oldřich Pytela ◽  
Aleš Halama
Keyword(s):  
Inductive Effect ◽  
Chemical Shifts ◽  
Quantitative Description ◽  
Substituent Effects ◽  
Intersection Point ◽  
Chemometric Analysis ◽  
Reaction Centre ◽  
Substituent Constant ◽  
Modified Method ◽  
Substituted Benzoic Acids

The paper deals with chemometric analysis of the inductive effect. The notion of inductive effect is discussed, and unambiguous definitions are given for the notions of triad: reaction centre-basic skeleton-substituent, and the therewith connected definitions of inductive effect. For a quantitative description of inductive effect 7 types of chemical models were selected including noncyclic compounds, cyclic, and bicyclic compounds, derivatives of quinuclidine, 3-substituted benzoic acids, sulfonamides and pyridines. Altogether 139 sets of experimental data from literature have been used including altogether 1 294 points (9.3 points per set, 5 points at least) reflecting substituent effects of 34 substituents. It has been found that for a standard model the dissociation of substituted bicycloalkanecarboxylic acids only is satisfactory, all the other models reflecting also the mesomeric effects to variable extent (up to 10%). A distinctly different substitution behaviour was observed with 19F and 13C NMR chemical shifts of 4-substituted 1-fluoro- or 1-methylbicyclo[2.2.2]octanes. The earlier suggested model of substituent effects based on different way of transmission of substituent effects (3 classes) has been used for separating the inductive and mesomeric effects: it is mathematically presented as a set of straight lines with the intersection point at the so-called isoeffect substituent constant. Using the modified method of conjugated deviations a chemometric scale has been created for the inductive effect which agrees very well with the conventional scales given in literature; the only differences were observed for F and CH=O substituents (which are overestimated and underestimated, respectively, in literature). In the context given the inductive effect appears as a fundamental quantity forming a basis for quantitative description of other effects transferred by electrons.

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