Collection of Czechoslovak Chemical Communications - digital archive 

Crossref Cited-by Linking

• Vlasov Vladislav M.: Simple method for determining of the isokinetic temperature value for the SNAr reactions in solution. J of Physical Organic Chem 2018, 31. <https://doi.org/10.1002/poc.3723>
• Vlasov Vladislav M.: Influence of the activation entropy on the change of the isokinetic temperature in the SN2 reactions in solution. Monatsh Chem 2018, 149, 2161. <https://doi.org/10.1007/s00706-018-2321-9>
• Garvín Alfonso, Ibarz Raquel, Ibarz Albert: Kinetic and thermodynamic compensation. A current and practical review for foods. Food Research International 2017, 96, 132. <https://doi.org/10.1016/j.foodres.2017.03.004>
• Rudakov Elisey S.: Mechanisms of alkane CH-activation: The 5/6 effect, single-factor compensation effect, strongest reactant and earliest transition state. A puzzle of Shilov reaction. Journal of Molecular Catalysis A: Chemical 2017, 426, 465. <https://doi.org/10.1016/j.molcata.2016.07.034>
• Oelgemöller Michael, Hoffmann Norbert: Studies in organic and physical photochemistry – an interdisciplinary approach. Org. Biomol. Chem. 2016, 14, 7392. <https://doi.org/10.1039/C6OB00842A>
• Pan Animesh, Biswas Tapas, Rakshit Animesh K., Moulik Satya P.: Enthalpy–Entropy Compensation (EEC) Effect: A Revisit. J. Phys. Chem. B 2015, 119, 15876. <https://doi.org/10.1021/acs.jpcb.5b09925>
• Vlasov Vladislav M., Kornakova Tatyana A.: Isokinetic relationships for SNAr reactions in different solvents. J of Physical Organic Chem 2013, 26, 131. <https://doi.org/10.1002/poc.2954>
• Vlasov Vladislav M.: Varying the activation parameters as a method of determining whether there is an isokinetic relationship among the bimolecular nucleophilic reactions of benzene derivatives in solution. Monatsh Chem 2013, 144, 41. <https://doi.org/10.1007/s00706-012-0765-x>
• Shi Yue, Zhu Crystal Z., Martin Stephen F., Ren Pengyu: Probing the Effect of Conformational Constraint on Phosphorylated Ligand Binding to an SH2 Domain Using Polarizable Force Field Simulations. J. Phys. Chem. B 2012, 116, 1716. <https://doi.org/10.1021/jp210265d>
• Galwey Andrew K., Bettany David G., Mortimer Michael: Kinetic compensation effects observed during oxidation of carbon monoxide on γ‐alumina supported palladium, platinum, and rhodium metal catalysts: Toward a mechanistic explanation. Int J of Chemical Kinetics 2006, 38, 689. <https://doi.org/10.1002/kin.20202>
• Bunten Kevin A., Po? Anthony J.: Multi-mechanism linear free energy relationships and isoequilibrium or isokinetic temperatures. New J. Chem. 2006, 30, 1638. <https://doi.org/10.1039/b603023h>
• Ouvrard Carole, Berthelot Michel, Lamer Thierry, Exner Otto: A Program for Linear Regression with a Common Point of Intersection:  The Isokinetic Relationship. J. Chem. Inf. Comput. Sci. 2001, 41, 1141. <https://doi.org/10.1021/ci000089s>
• Liu Lei, Guo Qing-Xiang: Isokinetic Relationship, Isoequilibrium Relationship, and Enthalpy−Entropy Compensation. Chem. Rev. 2001, 101, 673. <https://doi.org/10.1021/cr990416z>
• Bel'skii V. E.: Isokinetic relationships for nucleophilic substitution reactions at the saturated carbon atom. Reactions in aqueous solutions. Russ Chem Bull 2000, 49, 806. <https://doi.org/10.1007/BF02494700>
• Bunce Nigel J., Forber Christine L.: On the Correlation between ΔH‡ vs ΔS‡ in the thermal cis-to-trans isomerization of azobenzenes. Journal of Chemical Research 2000, 2000, 36. <https://doi.org/10.3184/030823400103165608>
• Fernandez Anthony, Reyes Clementina, Prock Alfred, Giering Warren P.: Exploring Ligand Effects through Isoequilibrium Phenomena:  The Quantitative Analysis of Ligand Effects. Organometallics 1998, 17, 2503. <https://doi.org/10.1021/om971041f>
• Exner Otto: How to get wrong results from good experimental data: a survey of incorrect applications of regression. J. Phys. Org. Chem. 1997, 10, 797. <https://doi.org/10.1002/(SICI)1099-1395(199711)10:11<797::AID-PCA951>3.0.CO;2-K>
• Connors Kenneth A.: The Stability of Cyclodextrin Complexes in Solution. Chem. Rev. 1997, 97, 1325. <https://doi.org/10.1021/cr960371r>
• Duca D., Frusteri F., Parmaliana A., Deganello G.: Selective hydrogenation of acetylene in ethylene feedstocks on Pd catalysts. Applied Catalysis A: General 1996, 146, 269. <https://doi.org/10.1016/S0926-860X(96)00145-7>
• Nongkynrih Irona, Mahanti Mahendra K: Kinetics of Oxidation of Cyclic Alcohols by Quinolinium Dichromate. Bulletin of the Chemical Society of Japan 1996, 69, 1403. <https://doi.org/10.1246/bcsj.69.1403>
• Li Jianjun, Carr Peter W.: Extra-thermodynamic relationships in chromatography enthalpy-entropy compensation in gas chromatography. Journal of Chromatography A 1994, 670, 105. <https://doi.org/10.1016/0021-9673(94)80285-8>
• Nongkynrih Irona, Mahanti Mahendra K: Kinetics and Mechanism of the Oxidative Cleavage of Unsaturated Acids by Quinolinium Dichromate. Bulletin of the Chemical Society of Japan 1994, 67, 2320. <https://doi.org/10.1246/bcsj.67.2320>
• Exner Otto: The reactivity–selectivity principle: redefinition and reexamination on an experimental basis. J. Chem. Soc., Perkin Trans. 2 1993, 973. <https://doi.org/10.1039/P29930000973>
• Exner Otto, Slanina Zdeněk: Thermodynamic and energy functions of fluorinated benzenes: their significance in correlation analysis. Thermochimica Acta 1990, 159, 67. <https://doi.org/10.1016/0040-6031(90)80094-F>
• Bunce N.J., Landers J.P., Nakai J.S., Winhall M.J., Safe S.H.: In vitro thermal inactivation of hepatic Ah receptors from several mammalian species. Toxicology in Vitro 1990, 4, 87. <https://doi.org/10.1016/0887-2333(90)90028-R>
• Linert Wolfgang, Han Liang-feng, Lukovits Istvan: The use of the isokinetic relationship and molecular mechanics to investigate molecular interactions in inclusion complexes of cyclodextrins. Chemical Physics 1989, 139, 441. <https://doi.org/10.1016/0301-0104(89)80156-9>
• Linert Wolfgang: The isokinetic relationship. X. Experimental examples to the relationship between isokinetic temperatures and active heat bath frequencies. Chemical Physics 1989, 129, 381. <https://doi.org/10.1016/0301-0104(89)85008-6>
• Linert W., Jaworski J.S.: A re-examination of temperature dependent reduction potentials of quinones from the point of view of the isokinetic relationship. Electrochimica Acta 1988, 33, 1713. <https://doi.org/10.1016/0013-4686(88)85004-7>
• Linert Wolfgang, Sapunov Valentin N.: The isokinetic relationship. IX. Connections to linear free energy relationships. Chemical Physics 1988, 119, 265. <https://doi.org/10.1016/0301-0104(88)87189-1>
• Linert W.: The isokinetic relationship. VII. Statistical analyses and examples for unimolecular reaction systems. Inorganica Chimica Acta 1988, 141, 233. <https://doi.org/10.1016/S0020-1693(00)83915-8>
• Halpern Jack: Determination of transition metal-alkyl bond dissociation energies from kinetic measurements. Polyhedron 1988, 7, 1483. <https://doi.org/10.1016/S0277-5387(00)81776-3>
• Halpern Jack: Compensation Effects in the Activation Parameters for the Homolytic Dissociation of Transition Metal–Alkyl Bonds. Bulletin of the Chemical Society of Japan 1988, 61, 13. <https://doi.org/10.1246/bcsj.61.13>
• Akhlaq M. S., Grossmann N., Pasbrig E., Fanghänel E.: Zur Kupplung von 4‐substituierten 2‐Pyrazolin‐5‐onen mit p‐Chinondiiminkationen; Nachweis isokinetischer Beziehungen. J. Prakt. Chem. 1987, 329, 217. <https://doi.org/10.1002/prac.19873290210>
• Linert Wolfgang: The isokinetic relationship. VIII. Investigation of unimolecular reaction systems. Chemical Physics 1987, 116, 381. <https://doi.org/10.1016/0301-0104(87)80206-9>
• Linert Wolfgang: The isokinetic relationship. V. Investigation of Bimolecular reaction systems. Chemical Physics 1987, 114, 449. <https://doi.org/10.1016/0301-0104(87)85059-0>
• Linert Wolfgang: The isokinetic relationship. VI. Equilibrium systems. Chemical Physics 1987, 114, 457. <https://doi.org/10.1016/0301-0104(87)85060-7>
• Lewis Nita A., Ray Amanda M.: Solvent effects on redox reactions. 2. The Cr(II) reduction of tris(pentane-2,4-dionato)cobalt(lII) in water/acetone solvent mixtures. Inorganica Chimica Acta 1987, 132, 49. <https://doi.org/10.1016/S0020-1693(00)83989-4>
• Russell S.T., Warshel A.: Calculations of electrostatic energies in proteins. Journal of Molecular Biology 1985, 185, 389. <https://doi.org/10.1016/0022-2836(85)90411-5>
• Thomas C. W., Leveson L. L.: Acid‐catalyzed hydrolysis of some diazoacetophenones in aqueous dioxan. Int J of Chemical Kinetics 1983, 15, 25. <https://doi.org/10.1002/kin.550150104>
• Giese Bernd, Lee Woo-Bung: Experimental evidence for a correlation between isoselective and isokinetic temperatures. Tetrahedron Letters 1982, 23, 3561. <https://doi.org/10.1016/S0040-4039(00)87669-8>
• Giese Bernd, Stellmach Joachim: Temperatureinfluß auf die Selektivität von σ‐Radikalen. Chem. Ber. 1980, 113, 3294. <https://doi.org/10.1002/cber.19801131017>
• Beezer Anthony E, Hunter William H, Storey David E: Quantitative structure-activity relationships: the Van't Hoff heats of transfer of resorcinol monoethers from water to n-octanol. Journal of Pharmacy and Pharmacology 1980, 32, 815. <https://doi.org/10.1111/j.2042-7158.1980.tb13082.x>
• Giese Bernd, Keller Karla: Das Reaktivitäts‐Selektivitätsprinzip, 4. Die Selektivität von Alkyl‐Radikalen im BrCCl 3 /CCl 4 ‐Konkurrenzsystem. Chem. Ber. 1979, 112, 1743. <https://doi.org/10.1002/cber.19791120524>
• Castro Bertrand, Nacro Mouhoussine, Selve Claude: Sels d'atdp—20. Tetrahedron 1979, 35, 627. <https://doi.org/10.1016/0040-4020(79)87007-6>
• Giese Bernd, Stellmach Joachim, Exner Otto: Application of the isoselective relationship to diels-alder reactions. Tetrahedron Letters 1979, 20, 2343. <https://doi.org/10.1016/S0040-4039(01)93968-1>
• Exner Otto, Giese Bernd: Die Anwendungsbreite der isoselektiven Beziehung. Angew. Chem. 1978, 90, 816. <https://doi.org/10.1002/ange.19780901026>
• Exner Otto, Giese Bernd: Scope of Application of the Isoselective Relationship. Angew. Chem. Int. Ed. Engl. 1978, 17, 775. <https://doi.org/10.1002/anie.197807751>
• Giese Bernd: Grundlagen und Grenzen des Reaktivitäts‐Selektivitätsprinzips. Angewandte Chemie 1977, 89, 162. <https://doi.org/10.1002/ange.19770890307>
• Giese Bernd: Basis and Limitations of the Reactivity‐Selectivity Principle. Angew. Chem. Int. Ed. Engl. 1977, 16, 125. <https://doi.org/10.1002/anie.197701253>
• EXNER O.: ChemInform Abstract: STATISTICS OF THE ENTHALPY‐ENTROPY RELATIONSHIP PART 5, THE ENTHALPY‐ENTROPY RELATIONSHIP IN ORGANIC REACTIONS. Chemischer Informationsdienst 1975, 6. <https://doi.org/10.1002/chin.197549113>