Cover Picture: Ionophoric Properties of [14]Tetraazaannulene Derivatives and Substituent Effect on the Cation-selectivity (Electroanalysis 7/2017)

T. M. Kawakami; M. Obita; T. Tsujinaka; A. Higashikado; T. Moriuchi

doi:10.1002/elan.201780701

Ionophoric Properties of [14]Tetraazaannulene Derivatives and Substituent Effect on the Cation-selectivity

Electroanalysis ◽

10.1002/elan.201700011 ◽

2017 ◽

Vol 29 (7) ◽

pp. 1712-1720 ◽

Cited By ~ 1

Author(s):

T. M. Kawakami ◽

M. Obita ◽

T. Tsujinaka ◽

A. Higashikado ◽

T. Moriuchi

Keyword(s):

Substituent Effect ◽

Cation Selectivity

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Substituent effect on wave numbers of C=O valence vibrations in ferrocene derivatives

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19831635 ◽

1983 ◽

Vol 48 (6) ◽

pp. 1635-1646 ◽

Cited By ~ 6

Author(s):

Alexander Perjéssy ◽

Štefan Toma

Keyword(s):

Linear Correlation ◽

Substituent Effect ◽

Empirical Relation ◽

Ferrocene Derivatives ◽

Wave Numbers ◽

Complex Structural ◽

Transmission Factors

Wave numbers of C=O valence vibrations of 83 ferrocene derivatives have been measured in tetrachloromethane. For a series of 154 compounds containing ferrocene skeleton linear correlation has been found between wave numbers of C=O vibration and X+(R) constants of structural fragments in the sense of modified and extended Seth-Paul-Van Duyse equation. Validity has been verified of the recently derived empirical relation for calculation of the X+(R) constants of complex structural fragments from values of constants of substituents and transmission factors for simple structural groupings. The transmission factors γ and π' for 1,3- and 1,1'-ferrocene system have been found to be well applicable to calculation of constants of structural fragments containing ferrocene skeleton.

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Ionic dimerisation of trifluoropropenenitrile and its addition reactions with methyl trifluoropropenoate

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19800406 ◽

1980 ◽

Vol 45 (2) ◽

pp. 406-414 ◽

Cited By ~ 4

Author(s):

Jiří Svoboda ◽

Oldřich Paleta ◽

Václav Dědek

Keyword(s):

Reaction Mechanism ◽

Proton Transfer ◽

Substituent Effect ◽

Solvent Molecule ◽

Addition Product ◽

Potassium Fluoride ◽

Relative Reactivity ◽

Addition Reactions ◽

Tertiary Amines ◽

Optimum Conditions

Dimerisation of trifluoropropenenitrile (I) in the presence of potassium fluoride and tertiary amines afforded a mixture of stereoisomeric perfluoro-4-methyl-pentenedinitriles (II), higher-boiling compounds, and 2,3,3,3-tetrafluoropropanenitrile (III) which arises by proton transfer from the solvent molecule. Under optimum conditions, product II was obtained in about 50% yield. Reaction of the nitrile I with methyl trifluoropropenoate (IV) gave, besides the dimers II and V, the product of addition of the nitrile I to the propenoate, IV, i.e. methyl 4-cyanoperfluoro-2-pentenoate (VI), and the addition product of the propenoate IV to the nitrile I, i.e. methyl 4-cyanoperfluoro-2-methyl-3-butenoate (VII). The relative reactivity if I and IV is discussed. The ratio of stereoisomers in II, V, VI and VII indicates that the magnitude of the steric substituent effect, operating in the reaction mechanism, decreases in the order -CFCF3.(COOCH3) > -CFCF3(CN) > -COOCH3 > -CN.

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Perturbation theory of substituent effect. Importance of the field effect in transmission of the substituent effect

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc19801655 ◽

1980 ◽

Vol 45 (6) ◽

pp. 1655-1661 ◽

Cited By ~ 1

Author(s):

Robert Ponec

Keyword(s):

Perturbation Theory ◽

Carboxylic Acids ◽

Quantum Chemical ◽

Substituent Effect ◽

Field Effect ◽

Adequate Description ◽

Meta Position ◽

Unsaturated Carboxylic Acids

Various quantum chemical approaches to the problem of transmission of the substituent effect were compared. It was shown that inclusion of the electronic repulsion (field effect) was necessary to give a true picture of differences in ρ constants for reactions of the cis and trans isomers of substituted unsaturated carboxylic acids; the same holds for an adequate description of transmission of the substituent effect from the meta position on a given skeleton.

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Kinetic Study of Hydrolysis of Benzoates. Part XXVI. Variation of the Substituent Effect with Solvent in Alkaline Hydrolysis of Substituted Alkyl Benzoates

Collection of Czechoslovak Chemical Communications ◽

10.1135/cccc20061557 ◽

2006 ◽

Vol 71 (11-12) ◽

pp. 1557-1570 ◽

Cited By ~ 10

Author(s):

Vilve Nummert ◽

Mare Piirsalu ◽

Ilmar A. Koppel

Keyword(s):

Kinetic Study ◽

Alkaline Hydrolysis ◽

Rate Constants ◽

Substituent Effect ◽

Substituent Effects ◽

Alkyl Substituent ◽

Solvent Parameters ◽

Substituent Constants ◽

Hydrolysis Of ◽

Main Factor

The second-order rate constants k2 (dm3 mol-1 s-1) for the alkaline hydrolysis of substituted alkyl benzoates C6H5CO2R have been measured spectrophotometrically in aqueous 0.5 M Bu4NBr at 50 and 25 °C (R = CH3, CH2Cl, CH2CN, CH2C≡CH, CH2C6H5, CH2CH2Cl, CH2CH2OCH3, CH2CH3) and in aqueous 5.3 M NaClO4 at 25 °C (R = CH3, CH2Cl, CH2CN, CH2C≡CH). The dependence of the alkyl substituent effects on different solvent parameters was studied using the following equations: ∆ log k = c0 + c1σI + c2EsB + c3∆E + c4∆Y + c5∆P + c6∆EσI + c7∆YσI + c8∆PσI ∆ log k = c0 + c1σ* + c2EsB + c3∆E + c4∆Y + c5∆P + c6∆Eσ* + c7∆Yσ* + c8∆Pσ* . ∆ log k = log kR - log kCH3. σI and σ* are the Taft inductive and polar substituent constants. E, Y and P are the solvent electrophilicity, polarity and polarizability parameters, respectively. In the data treatment ∆E = ES - EH2O , ∆Y = YS - YH2O , ∆P = PS - PH2O were used. The solvent electrophilicity, E, was found to be the main factor responsible for changes in alkyl substituent effects with medium. When σI constants were used, variation of the polar term of alkyl substituents with the solvent electrophilicity E was found to be similar to that observed earlier for meta and para substituents, but twice less when σ* constants were used. The steric term for alkyl substituents was approximately independent of the solvent parameters.

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