Статті в журналах з теми "Intramolecular model"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Intramolecular model".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Feldman, J. L., J. Q. Broughton, L. L. Boyer, D. E. Reich, and M. D. Kluge. "Intramolecular-force-constant model forC60." Physical Review B 46, no. 19 (November 15, 1992): 12731–36. http://dx.doi.org/10.1103/physrevb.46.12731.
Повний текст джерелаHu, Wenbing, Daan Frenkel, and Vincent B. F. Mathot. "Intramolecular Nucleation Model for Polymer Crystallization." Macromolecules 36, no. 21 (October 2003): 8178–83. http://dx.doi.org/10.1021/ma0344285.
Повний текст джерелаFeldman, J. L., J. Q. Broughton, L. L. Boyer, D. E. Reich, and M. D. Kluge. "Erratum: Intramolecular-force-constant model forC60." Physical Review B 47, no. 15 (April 15, 1993): 10058. http://dx.doi.org/10.1103/physrevb.47.10058.
Повний текст джерелаDang, Liem X., and B. Montgomery Pettitt. "Simple intramolecular model potentials for water." Journal of Physical Chemistry 91, no. 12 (June 1987): 3349–54. http://dx.doi.org/10.1021/j100296a048.
Повний текст джерелаUzer, T., and James T. Hynes. "Intramolecular energy transfer in simple model organometallics." Journal of Physical Chemistry 90, no. 16 (July 1986): 3524–27. http://dx.doi.org/10.1021/j100407a014.
Повний текст джерелаOlson, Ryan M., Aleksandr V. Marenich, Christopher J. Cramer, and Donald G. Truhlar. "Charge Model 4 and Intramolecular Charge Polarization." Journal of Chemical Theory and Computation 3, no. 6 (October 25, 2007): 2046–54. http://dx.doi.org/10.1021/ct7001607.
Повний текст джерелаIshenko, S. Ia, M. V. Vener, and V. M. Mamaev. "Two-dimensional model of intramolecular hydrogen bond." Theoretica Chimica Acta 68, no. 5 (November 1985): 351–62. http://dx.doi.org/10.1007/bf00529056.
Повний текст джерелаSpellmeyer, D. C., and K. N. Houk. "Force-field model for intramolecular radical additions." Journal of Organic Chemistry 52, no. 6 (March 1987): 959–74. http://dx.doi.org/10.1021/jo00382a001.
Повний текст джерелаLI, JUAN-QIN, XIANG-YUAN LI, and FENG WANG. "A THEORETICAL STUDY ON DUAL FLUORESCENCE OF 4-DIMETHYLAMINOPYRIDINE BY POLARIZABLE CONTINUUM MODEL." Journal of Theoretical and Computational Chemistry 07, no. 04 (August 2008): 821–32. http://dx.doi.org/10.1142/s0219633608004143.
Повний текст джерелаPolimeno, Antonino, Antonio Barbon, Pier Luigi Nordio, and Wolfgang Rettig. "Stochastic Model for Solvent-Assisted Intramolecular Charge-Transfer." Journal of Physical Chemistry 98, no. 47 (November 1994): 12158–68. http://dx.doi.org/10.1021/j100098a008.
Повний текст джерелаLuigi Nordio, Pier, Antonino Polimeno, and Giacomo Saielli. "Theoretical model of photoinduced intramolecular charge transfer processes." Journal of Photochemistry and Photobiology A: Chemistry 105, no. 2-3 (May 1997): 269–76. http://dx.doi.org/10.1016/s1010-6030(96)04569-8.
Повний текст джерелаVan de Vijver, Ruben, Maarten K. Sabbe, Marie-Françoise Reyniers, Kevin M. Van Geem, and Guy B. Marin. "Ab initio derived group additivity model for intramolecular hydrogen abstraction reactions." Physical Chemistry Chemical Physics 20, no. 16 (2018): 10877–94. http://dx.doi.org/10.1039/c7cp07771h.
Повний текст джерелаHoppmann, Christian, Ronald Kühne, and Michael Beyermann. "Intramolecular bridges formed by photoswitchable click amino acids." Beilstein Journal of Organic Chemistry 8 (June 13, 2012): 884–89. http://dx.doi.org/10.3762/bjoc.8.100.
Повний текст джерелаSugden, Isaac J., Claire S. Adjiman, and Constantinos C. Pantelides. "Accurate and efficient representation of intramolecular energy in ab initio generation of crystal structures. II. Smoothed intramolecular potentials." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 75, no. 3 (May 23, 2019): 423–33. http://dx.doi.org/10.1107/s2052520619005778.
Повний текст джерелаSumpter, Bobby G., and Donald L. Thompson. "Studies of the intramolecular dynamics of model polyatomic molecules." Journal of Chemical Physics 86, no. 5 (March 1987): 2805–17. http://dx.doi.org/10.1063/1.452082.
Повний текст джерелаKolafa, Jiří. "A Polarizable Three-Site Water Model with Intramolecular Polarizability." Collection of Czechoslovak Chemical Communications 73, no. 4 (2008): 507–17. http://dx.doi.org/10.1135/cccc20080507.
Повний текст джерелаSingh, Serjinder, Sarita Nagrath, and Minakshi Chanana. "An intramolecular NADH model containing an activating acidic group." Journal of the Chemical Society, Chemical Communications, no. 4 (1986): 282. http://dx.doi.org/10.1039/c39860000282.
Повний текст джерелаSumpter, Bobby G., and Donald L. Thompson. "Intramolecular vibrational energy flow in model four‐atom systems." Journal of Chemical Physics 82, no. 10 (May 15, 1985): 4557–65. http://dx.doi.org/10.1063/1.448712.
Повний текст джерелаKurzyński, Michal/. "A model of reversible reaction with slow intramolecular relaxation." Journal of Chemical Physics 101, no. 1 (July 1994): 255–64. http://dx.doi.org/10.1063/1.468177.
Повний текст джерелаPrill, Dragica, Pavol Juhás, Martin U. Schmidt, and Simon J. L. Billinge. "Modelling pair distribution functions (PDFs) of organic compounds: describing both intra- and intermolecular correlation functions in calculated PDFs." Journal of Applied Crystallography 48, no. 1 (January 30, 2015): 171–78. http://dx.doi.org/10.1107/s1600576714026454.
Повний текст джерелаBaggioli, Alberto, Carlo A. Cavallotti, and Antonino Famulari. "Exploring short intramolecular interactions in alkylaromatic substrates." Physical Chemistry Chemical Physics 18, no. 42 (2016): 29616–28. http://dx.doi.org/10.1039/c6cp03323g.
Повний текст джерелаBilton, Clair, Frank H. Allen, Gregory P. Shields, and Judith A. K. Howard. "Intramolecular hydrogen bonds: common motifs, probabilities of formation and implications for supramolecular organization." Acta Crystallographica Section B Structural Science 56, no. 5 (October 1, 2000): 849–56. http://dx.doi.org/10.1107/s0108768100003694.
Повний текст джерелаISHDORJ, TSEREN-ONOLT, ION PETRE, and VLADIMIR ROGOJIN. "COMPUTATIONAL POWER OF INTRAMOLECULAR GENE ASSEMBLY." International Journal of Foundations of Computer Science 18, no. 05 (October 2007): 1123–36. http://dx.doi.org/10.1142/s0129054107005169.
Повний текст джерелаHasegawa, Taisuke, and Yoshitaka Tanimura. "A Polarizable Water Model for Intramolecular and Intermolecular Vibrational Spectroscopies." Journal of Physical Chemistry B 115, no. 18 (May 12, 2011): 5545–53. http://dx.doi.org/10.1021/jp111308f.
Повний текст джерелаVakhnenko, Oleksiy O. "Nonlinear model of intramolecular excitations on a multileg ladder lattice." Physical Review E 60, no. 3 (September 1, 1999): R2492—R2495. http://dx.doi.org/10.1103/physreve.60.r2492.
Повний текст джерелаCharonnat, Jeffrey, Nobuko Nishimura, Bruce Travers, and Jack Waas. "Novel Application of the Intramolecular Prins Reaction: (-)-Anisatin Model Study." Synlett 1996, no. 12 (December 1996): 1162–64. http://dx.doi.org/10.1055/s-1996-5718.
Повний текст джерелаZhang, Hong, Manhua Zhang, and Tao Shen. "Photoinduced intramolecular electron transfer in an anthraquinone-fluorescein-carbazole model." Journal of Photochemistry and Photobiology A: Chemistry 103, no. 1-2 (February 1997): 63–67. http://dx.doi.org/10.1016/s1010-6030(96)04490-5.
Повний текст джерелаDolata, Daniel P., and Laurence M. Harwood. "An axiomatic model of the intramolecular Diels-Alder furan reaction." Journal of the American Chemical Society 114, no. 27 (December 1992): 10738–46. http://dx.doi.org/10.1021/ja00053a009.
Повний текст джерелаPackard, B. Z., D. D. Toptygin, A. Komoriya, and L. Brand. "Profluorescent protease substrates: intramolecular dimers described by the exciton model." Proceedings of the National Academy of Sciences 93, no. 21 (October 15, 1996): 11640–45. http://dx.doi.org/10.1073/pnas.93.21.11640.
Повний текст джерелаGruebele, M. "Bose Statistics Triangle Rule Model for Intramolecular Vibrational Energy Redistribution." Journal of Physical Chemistry 100, no. 30 (January 1996): 12183–92. http://dx.doi.org/10.1021/jp960443i.
Повний текст джерелаMoran, Damian, Rebecca Jacob, Geoffrey P F. Wood, Michelle L Coote, Michael J Davies, Richard A J. O'Hair, Christopher J Easton, and Leo Radom. "Rearrangements in Model Peptide-Type Radicalsvia Intramolecular Hydrogen-Atom Transfer." Helvetica Chimica Acta 89, no. 10 (October 2006): 2254–72. http://dx.doi.org/10.1002/hlca.200690210.
Повний текст джерелаGeyer, Armin, Ursula Huchel, and Richard R. Schmidt. "Conformational analyses of model structures for intramolecular glycoside bond formation." Magnetic Resonance in Chemistry 37, no. 2 (February 1999): 145–48. http://dx.doi.org/10.1002/(sici)1097-458x(199902)37:2<145::aid-mrc418>3.0.co;2-f.
Повний текст джерелаHolt, Asbjørn, and Gunnar Karlström. "An intramolecular induction correction model of the molecular dipole moment." Journal of Computational Chemistry 29, no. 7 (2008): 1084–91. http://dx.doi.org/10.1002/jcc.20867.
Повний текст джерелаLerrick, Reinner I. "Sonication-Assisted Mitsunobu Etherification of Sterically Encumbered and Intramolecular Hydrogen Demanding Compounds: A Model towards Intramolecular MPV Reduction." IPTEK Journal of Proceedings Series, no. 4 (November 1, 2017): 1. http://dx.doi.org/10.12962/j23546026.y2017i4.3065.
Повний текст джерелаLeslie, DR, та S. Pantelidis. "Intramolecular Catalysis of Dialkyl ω-Aminoalkylphosphonate Hydrolysis". Australian Journal of Chemistry 47, № 3 (1994): 545. http://dx.doi.org/10.1071/ch9940545.
Повний текст джерелаAiraghi, Francesco, Andrea Fiorati, Giordano Lesma, Manuele Musolino, Alessandro Sacchetti та Alessandra Silvani. "The diketopiperazine-fused tetrahydro-β-carboline scaffold as a model peptidomimetic with an unusual α-turn secondary structure". Beilstein Journal of Organic Chemistry 9 (22 січня 2013): 147–54. http://dx.doi.org/10.3762/bjoc.9.17.
Повний текст джерелаSinha, Sneha, Chelsea Yang, Emily Wu, and William E. Acree. "Abraham Solvation Parameter Model: Examination of Possible Intramolecular Hydrogen-Bonding Using Calculated Solute Descriptors." Liquids 2, no. 3 (July 24, 2022): 131–46. http://dx.doi.org/10.3390/liquids2030009.
Повний текст джерелаHellou, Jocelyne, Gervais Bérubé, Michael J. Newlands, Alex G. Fallis, and Eric J. Gabe. "Intramolecular Diels–Alder reactions of cyclopentadiene systems: Model studies for the total synthesis of the capnellenes." Canadian Journal of Chemistry 66, no. 3 (March 1, 1988): 439–48. http://dx.doi.org/10.1139/v88-077.
Повний текст джерелаRAISSI, HEIDAR, FARZANEH FARZAD, SHAHIRA ESLAMDOOST, and FARIBA MOLLANIA. "CONFORMATIONAL PROPERTIES AND INTRAMOLECULAR HYDROGEN BONDING OF 3-AMINO-PROPENESELENAL: AN AB INITIO AND DENSITY FUNCTIONAL THEORY STUDIES." Journal of Theoretical and Computational Chemistry 12, no. 04 (June 2013): 1350025. http://dx.doi.org/10.1142/s0219633613500259.
Повний текст джерелаTcherkez, Guillaume, Graham Farquhar, Franz Badeck, and Jaleh Ghashghaie. "Theoretical considerations about carbon isotope distribution in glucose of C3 plants." Functional Plant Biology 31, no. 9 (2004): 857. http://dx.doi.org/10.1071/fp04053.
Повний текст джерелаSkalski, Bohdan, Grazyna Wenska, Stefan Paszyc, and Zdzislaw Stefaniak. "Photocycloaddition of cytosine to 5-methoxyuracil in dinucleotide model compound." Canadian Journal of Chemistry 66, no. 5 (May 1, 1988): 1027–31. http://dx.doi.org/10.1139/v88-170.
Повний текст джерелаKarpińska, Grażyna, and Aleksander P. Mazurek. "Studies on Activation of H3 Histamine Receptor: A Mechanistic Model." Zeitschrift für Naturforschung C 50, no. 1-2 (February 1, 1995): 143–47. http://dx.doi.org/10.1515/znc-1995-1-221.
Повний текст джерелаJezierska, Aneta, Peter M. Tolstoy, Jarosław J. Panek, and Aleksander Filarowski. "Intramolecular Hydrogen Bonds in Selected Aromatic Compounds: Recent Developments." Catalysts 9, no. 11 (October 30, 2019): 909. http://dx.doi.org/10.3390/catal9110909.
Повний текст джерелаSonnay, Marjorie, and Felix Zelder. "Stabilizing intramolecular cobalt–imidazole coordination with a remote methyl group in the backbone of a cofactor B12–protein model." Dalton Transactions 47, no. 31 (2018): 10443–46. http://dx.doi.org/10.1039/c8dt01298a.
Повний текст джерелаŠolc, Milan. "A stochastic model of decomposition of selectively excited polyatomic molecules." Collection of Czechoslovak Chemical Communications 55, no. 7 (1990): 1647–52. http://dx.doi.org/10.1135/cccc19901647.
Повний текст джерелаTang, Ting-Hua, Dennis M. Whitfield, Stephen P. Douglas, Jiri J. Krepinsky, and Imre G. Csizmadia. "Differential reactivity of carbohydrate hydroxyls in glycosylations. I. Intramolecular interaction of the 5′-hydroxyl group with the heteroaromatic base in a model compound of 2′-deoxycytidine." Canadian Journal of Chemistry 70, no. 9 (September 1, 1992): 2434–48. http://dx.doi.org/10.1139/v92-309.
Повний текст джерелаDenayer, Mats, Jelle Vekeman, Frederik Tielens, and Frank De Proft. "Towards a predictive model for polymer solubility using the noncovalent interaction index: polyethylene as a case study." Physical Chemistry Chemical Physics 23, no. 44 (2021): 25374–87. http://dx.doi.org/10.1039/d1cp04346c.
Повний текст джерелаNovikov, Eugene, Andrzej Molski, and Noël Boens. "Identifiability of a model for diffusion-mediated intramolecular excited-state quenching." Journal of Chemical Physics 112, no. 12 (March 22, 2000): 5348–52. http://dx.doi.org/10.1063/1.481104.
Повний текст джерелаKende, Andrew S., and Cynthia A. Smith. "Synthesis of a Calicheamicin Deoxyaglycone Model by an Intramolecular Acetylide Cyclization." Tetrahedron Letters 29, no. 34 (January 1988): 4217–20. http://dx.doi.org/10.1016/s0040-4039(00)80458-x.
Повний текст джерелаZhang, Aiqin, Jiuli Zhang, Qiliang Pan, Shuhua Wang, Husheng Jia, and Bingshe Xu. "Synthesis, photoluminescence and intramolecular energy transfer model of a dysprosium complex." Journal of Luminescence 132, no. 4 (April 2012): 965–71. http://dx.doi.org/10.1016/j.jlumin.2011.11.023.
Повний текст джерела