Статті в журналах з теми "Bond exchange reaction"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Bond exchange reaction".
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.
Zhao, Dongbing, Wen-Tao Zhao та Fang Gao. "Recent Progress in σ-Bond Cross-Exchange Reactions to Access Diverse Silacycles". Synlett 29, № 20 (30 серпня 2018): 2595–600. http://dx.doi.org/10.1055/s-0037-1610266.
Повний текст джерелаArisawa, Mieko, Tomoki Yamada, Saori Tanii, Yuta Kawada, Hisako Hashimoto, and Masahiko Yamaguchi. "Rhodium-catalyzed P–P bond exchange reaction of diphosphine disulfides." Chemical Communications 52, no. 93 (2016): 13580–83. http://dx.doi.org/10.1039/c6cc07302f.
Повний текст джерелаYang, Xichuan, Mikael Kritikos, Björn Åkermark, and Licheng Sun. "Axial ligand exchange reaction on ruthenium phthalocyanines." Journal of Porphyrins and Phthalocyanines 09, no. 04 (April 2005): 248–55. http://dx.doi.org/10.1142/s1088424605000319.
Повний текст джерелаSutrisno, Sutrisno, and Rahayu Ningtiyas. "DERERMINANTS OF ISLAMIC BOND MARKET REACTION Empirical Study of Islamic Bond in Indonesia." Jurnal Apresiasi Ekonomi 9, no. 2 (May 31, 2021): 152–58. http://dx.doi.org/10.31846/jae.v9i2.379.
Повний текст джерелаRyabov, Alexander D. "The Exchange of Cyclometalated Ligands." Molecules 26, no. 1 (January 3, 2021): 210. http://dx.doi.org/10.3390/molecules26010210.
Повний текст джерелаLI, PING, XIAOYAN XIE, YUXIANG BU, WEIHUA WANG, NANA WANG, JUNYOU SHI, and ZHAOXIA MOU. "THEORETICAL STUDIES ON THE COUPLING INTERACTIONS AND SELF-EXCHANGE REACTION MECHANISMS IN THE COMPLEXES OF NO WITH ONH AND NOH." Journal of Theoretical and Computational Chemistry 07, no. 03 (June 2008): 435–46. http://dx.doi.org/10.1142/s0219633608003848.
Повний текст джерелаDENG, XIN, LIN GE, and XUAN WU. "SPILLOVER EFFECT OF THE FEDERAL RESERVE’S FORWARD GUIDANCE ON CHINA’S FINANCIAL MARKETS: FROM MECHANISM ANALYSIS TO EMPIRICAL TEST." Singapore Economic Review 67, no. 02 (October 7, 2021): 603–34. http://dx.doi.org/10.1142/s0217590821500612.
Повний текст джерелаHarcourt, Richard D., and Rickie Ng. "Valence bond representation for the hydrogen atom exchange reaction." Journal of Physical Chemistry 97, no. 47 (November 1993): 12210–14. http://dx.doi.org/10.1021/j100149a019.
Повний текст джерелаCasey, W. H. "A view of reactions at mineral surfaces from the aqueous phase." Mineralogical Magazine 65, no. 3 (June 2001): 323–37. http://dx.doi.org/10.1180/002646101300119439.
Повний текст джерелаLutfiyah, Lailatul, and Mu’minatus Sholichah. "Pengaruh Nilai Sukuk Dan Risiko Sukuk Terhadap Reaksi Pasar Modal." Journal of Culture Accounting and Auditing 1, no. 1 (July 14, 2022): 107. http://dx.doi.org/10.30587/jcaa.v1i1.4233.
Повний текст джерелаFolga, E., and T. Ziegler. "A theoretical study on the activation of hydrogen–hydrogen and hydrogen–alkyl bonds by electron-poor early transition metals." Canadian Journal of Chemistry 70, no. 2 (February 1, 1992): 333–42. http://dx.doi.org/10.1139/v92-047.
Повний текст джерелаPulatov, Khayrulla, Rano Nazirova, Umida Sharipova, Alisher Yuldashev, Aziza Usmonova, Shakhriyor Sattorov, and Yorkinjon Ergashev. "Research new type of cation-exchange resin for waste water treatment." E3S Web of Conferences 497 (2024): 02035. http://dx.doi.org/10.1051/e3sconf/202449702035.
Повний текст джерелаJanzen, Alexander F., and Meehae Jang. "Isomerization, fluorine exchange, and stereoselective synthesis of cis- and trans-F2TePh3Cl: application of the coordination model of reaction mechanisms." Canadian Journal of Chemistry 67, no. 1 (January 1, 1989): 71–75. http://dx.doi.org/10.1139/v89-012.
Повний текст джерелаGiebler, Michael, Clemens Sperling, Simon Kaiser, Ivica Duretek, and Sandra Schlögl. "Epoxy-Anhydride Vitrimers from Aminoglycidyl Resins with High Glass Transition Temperature and Efficient Stress Relaxation." Polymers 12, no. 5 (May 17, 2020): 1148. http://dx.doi.org/10.3390/polym12051148.
Повний текст джерелаUhlig, Wolfram. "Zur gezielten Synthese funktionell substituierter Oligosilane aus Silyltriflaten und Aminosilyllithiumverbindungen / Tailor-Made Synthesis of Functional Substituted Oligosilanes from Silyl Triflates and (Aminosilyl)Lithium Compounds." Zeitschrift für Naturforschung B 58, no. 1 (January 1, 2003): 183–90. http://dx.doi.org/10.1515/znb-2003-0128.
Повний текст джерелаTao, Sheng, Enhui Ji, Lei Shi, Ning Liu, Liang Xu, and Bin Dai. "Copper-Catalyzed C–N Bond Exchange of N-Heterocyclic Substituents around Pyridine and Pyrimidine Cores." Synthesis 49, no. 23 (August 28, 2017): 5120–30. http://dx.doi.org/10.1055/s-0036-1590893.
Повний текст джерелаYu, Sheng-Sheng, Ramanarayanan Krishnamurthy, Facundo M. Fernández, Nicholas V. Hud, F. Joseph Schork, and Martha A. Grover. "Kinetics of prebiotic depsipeptide formation from the ester–amide exchange reaction." Physical Chemistry Chemical Physics 18, no. 41 (2016): 28441–50. http://dx.doi.org/10.1039/c6cp05527c.
Повний текст джерелаMais, Rimi Gusliana, Dea Maharani, and Agus Prasetyo. "Issuance Value, Issuance Rating and Life of Sharia Bond on Sharia Capital Market Reaction." JFBA: Journal of Financial and Behavioural Accounting 1, no. 1 (April 5, 2021): 83–92. http://dx.doi.org/10.33830/jfba.v1i1.2241.2021.
Повний текст джерелаWalewska, Małgorzata, Judith Baumgartner, and Christoph Marschner. "1,2- and 1,1-Migratory Insertion Reactions of Silylated Germylene Adducts." Molecules 25, no. 3 (February 6, 2020): 686. http://dx.doi.org/10.3390/molecules25030686.
Повний текст джерелаByrne, Aaron, Eduardo Bringa, Mario Del Pópolo, Jorge Kohanoff, Vanesa Galassi, and Niall English. "Mechanisms of Iodide–Triiodide Exchange Reactions in Ionic Liquids: A Reactive Molecular-Dynamics Exploration." International Journal of Molecular Sciences 20, no. 5 (March 5, 2019): 1123. http://dx.doi.org/10.3390/ijms20051123.
Повний текст джерелаSugiura, Takumi, Takurou Kanada, Daisuke Mori, Hiroyuki Sakai, Aya Shibata, Yoshiaki Kitamura, and Masato Ikeda. "Chemical stimulus-responsive supramolecular hydrogel formation and shrinkage of a hydrazone-containing short peptide derivative." Soft Matter 16, no. 4 (2020): 899–906. http://dx.doi.org/10.1039/c9sm01969c.
Повний текст джерелаArisawa, Mieko, and Masahiko Yamaguchi. "Rhodium-Catalyzed Synthesis of Organosulfur Compounds using Sulfur." Synlett 30, no. 14 (July 2, 2019): 1621–31. http://dx.doi.org/10.1055/s-0037-1611867.
Повний текст джерелаTachikawa, Hiroto. "SN2 and SN2′ reaction dynamics of cyclopropenyl chloride with halide ion A direct ab initio molecular dynamics (MD) study." Canadian Journal of Chemistry 83, no. 9 (September 1, 2005): 1597–605. http://dx.doi.org/10.1139/v05-176.
Повний текст джерелаYe, Chenqing, Yichun Xie, Liping Zheng, Yuxiang Lin, Weixiang Guo, and Xueqiang Qi. "The anode oxidation reaction in fuel cell: A DFT study." E3S Web of Conferences 267 (2021): 02054. http://dx.doi.org/10.1051/e3sconf/202126702054.
Повний текст джерелаMeyer, Matthias, Johannes Kadel, and Heinz Oberhammer. "Triazaphosphinine – Reaktionen, Zwitterionen, P–B-Austausch/ Triazaphosphinines – Reactions, Zwitter Ions, P – B-Exchange." Zeitschrift für Naturforschung B 43, no. 8 (August 1, 1988): 1010–16. http://dx.doi.org/10.1515/znb-1988-0816.
Повний текст джерелаGast, Rainer, Thomas Kaukorat, Ion Neda, and Reinhard Schmutzler. "Das 2-Halogen-5,6-benzo-1,3,2-dioxaphosphorinan-4-on-Ringsystem / The 2-Halogeno-5,6-benzo-1,3,2-dioxaphosphorinan-4-one Ring System." Zeitschrift für Naturforschung B 48, no. 7 (July 1, 1993): 867–74. http://dx.doi.org/10.1515/znb-1993-0703.
Повний текст джерелаBarth, Andreas, and Natalya Bezlyepkina. "P–O Bond Destabilization Accelerates Phosphoenzyme Hydrolysis of Sarcoplasmic Reticulum Ca2+-ATPase." Journal of Biological Chemistry 279, no. 50 (September 27, 2004): 51888–96. http://dx.doi.org/10.1074/jbc.m410867200.
Повний текст джерелаWu, Jian-Bo, Shu-Jia Li, Hong Liu, Hu-Jun Qian, and Zhong-Yuan Lu. "Dynamics and reaction kinetics of coarse-grained bulk vitrimers: a molecular dynamics study." Physical Chemistry Chemical Physics 21, no. 24 (2019): 13258–67. http://dx.doi.org/10.1039/c9cp01766f.
Повний текст джерелаBao, Junwei Lucas, Xin Zhang, and Donald G. Truhlar. "Barrierless association of CF2and dissociation of C2F4by variational transition-state theory and system-specific quantum Rice–Ramsperger–Kassel theory." Proceedings of the National Academy of Sciences 113, no. 48 (November 10, 2016): 13606–11. http://dx.doi.org/10.1073/pnas.1616208113.
Повний текст джерелаEl Hamidi, Sana, Malika Khnifira, El Mokhtar Lemdek, Redouan Hammal, Noureddine Barka, M’hamed Sadiq, Ahmed Benharref, Ahmed Chekroun, Hssaine Zgou та Mohamed Abdennouri. "Understanding the Mechanism and Selectivities of the Reaction of Meta-Chloroperbenzoic Acid and Dibromocarbene with β-Himachalene: A DFT Study". Heteroatom Chemistry 2020 (18 вересня 2020): 1–8. http://dx.doi.org/10.1155/2020/8885991.
Повний текст джерелаChen, Baolong, Xin Hu, and Xiaoqing Zhu. "Essential Rule Derived from Thermodynamics and Kinetics Studies of Benzopyran Compounds." Molecules 28, no. 24 (December 11, 2023): 8039. http://dx.doi.org/10.3390/molecules28248039.
Повний текст джерелаLee, Changmin, Eunhee Nam, Woosuk Lee, and Heeyeop Chae. "Hydrosilylation of Reactive Quantum Dots and Siloxanes for Stable Quantum Dot Films." Polymers 11, no. 5 (May 18, 2019): 905. http://dx.doi.org/10.3390/polym11050905.
Повний текст джерелаUndheim, Kjell. "Bond Formation at C8 in the Nucleoside and Nucleotide Purine Scaffold: An Informative Selection." Molecules 29, no. 8 (April 17, 2024): 1815. http://dx.doi.org/10.3390/molecules29081815.
Повний текст джерелаFrand, Alison R., and Chris A. Kaiser. "Two Pairs of Conserved Cysteines Are Required for the Oxidative Activity of Ero1p in Protein Disulfide Bond Formation in the Endoplasmic Reticulum." Molecular Biology of the Cell 11, no. 9 (September 2000): 2833–43. http://dx.doi.org/10.1091/mbc.11.9.2833.
Повний текст джерелаYe, Runyou, Maoshuai Zhu, Xufei Yan, Yang Long, Ying Xia, and Xiangge Zhou. "Pd(II)-Catalyzed C═C Bond Cleavage by a Formal Group-Exchange Reaction." ACS Catalysis 11, no. 14 (July 1, 2021): 8678–83. http://dx.doi.org/10.1021/acscatal.1c01850.
Повний текст джерелаNeves, Rui P. P., Pedro Alexandrino Fernandes, and Maria João Ramos. "Mechanistic insights on the reduction of glutathione disulfide by protein disulfide isomerase." Proceedings of the National Academy of Sciences 114, no. 24 (May 30, 2017): E4724—E4733. http://dx.doi.org/10.1073/pnas.1618985114.
Повний текст джерелаSwaddle, T. W. "Inorganic solution chemistry at elevated pressures." Canadian Journal of Physics 73, no. 5-6 (May 1, 1995): 258–66. http://dx.doi.org/10.1139/p95-037.
Повний текст джерелаRenodon-Corniere, Axelle, Tsutomu Mikawa, Naoyuki Kuwabara, Kentaro Ito, Dmitri Levitsky, Hiroshi Iwasaki, and Masayuki Takahashi. "Human Rad51 Protein Requires Higher Concentrations of Calcium Ions for D-Loop Formation than for Oligonucleotide Strand Exchange." International Journal of Molecular Sciences 25, no. 7 (March 24, 2024): 3633. http://dx.doi.org/10.3390/ijms25073633.
Повний текст джерелаList, Benjamin, Hui Zhou, and Pinglu Zhang. "The Silicon–Hydrogen Exchange Reaction: Catalytic Kinetic Resolution of 2-Substituted Cyclic Ketones." Synlett 32, no. 19 (October 15, 2021): 1953–56. http://dx.doi.org/10.1055/a-1670-5829.
Повний текст джерелаSoon, Julian Wong, Koji Oohora, and Takashi Hayashi. "A disulphide bond-mediated hetero-dimer of a hemoprotein and a fluorescent protein exhibiting efficient energy transfer." RSC Advances 12, no. 44 (2022): 28519–24. http://dx.doi.org/10.1039/d2ra05249k.
Повний текст джерелаZhou, Zhongqun, Yanning Zeng, Caili Yu, Haibo Chen, and Faai Zhang. "Mechanically robust, intrinsically self-healing crosslinked polymer enabled by dynamic urea bond exchange reaction." Smart Materials and Structures 29, no. 11 (October 8, 2020): 115041. http://dx.doi.org/10.1088/1361-665x/abb574.
Повний текст джерелаWark, Teresa A., та Douglas W. Stephan. "Rhodium induced titanium–sulfur bond cleavage: crystal and molecular structure of ((COD)Rh(μ-SMe))2". Canadian Journal of Chemistry 68, № 4 (1 квітня 1990): 565–69. http://dx.doi.org/10.1139/v90-086.
Повний текст джерелаWrackmeyer, Bernd, Christoph Bihlmayer, Khadija Shahid, and Wolfgang Milius. "Reaction of 9-Borabicyclo[3.3.1]nonane with Alkyn-1-yltin Compounds. Molecular Structure of the 9-Propyn-1-yl-9-borabicyclo[3.3.1]nonane Pyridine Adduct." Zeitschrift für Naturforschung B 64, no. 4 (April 1, 2009): 399–402. http://dx.doi.org/10.1515/znb-2009-0407.
Повний текст джерелаJones, William, Brett Swartz, and William Brennessel. "Lewis Acid Assisted C–CN Cleavage of Benzonitrile Using [(dippe)NiH]2." Synlett 29, no. 06 (July 20, 2017): 747–53. http://dx.doi.org/10.1055/s-0036-1590801.
Повний текст джерелаTiritiris, Ioannis, and Willi Kantlehner. "Crystal structure ofN,N,N′,N′,N′′,N′′-hexamethylguanidinium cyanate 1.5-hydrate." Acta Crystallographica Section E Crystallographic Communications 71, no. 12 (December 1, 2015): o1076—o1077. http://dx.doi.org/10.1107/s2056989015024317.
Повний текст джерелаMatsumoto, Mitsuru, Shigenobu Funahashi, and Hideo D. Takagi. "Electrochemical Electron Transfer Reactions of M(ttcn)23+/2+ (M = Co, Pd, Pt, Au; ttcn = 1,4,7-trithiacyclononane): the Relation of Reaction Volumes and Electron Transfer Rate Constants." Zeitschrift für Naturforschung B 54, no. 9 (September 1, 1999): 1138–46. http://dx.doi.org/10.1515/znb-1999-0909.
Повний текст джерелаCao, Dapeng, Qifang Li, Manxi Zhou, Lei Zhu, Zhimin Sun, and Zhenqing Yang. "Tri-Petal Lilac-Like Perylene: Asymmetrical Substituted Platform for Regioselective Ether-Exchange Reaction." Synlett 28, no. 16 (July 6, 2017): 2121–25. http://dx.doi.org/10.1055/s-0036-1590808.
Повний текст джерелаPokorny, Diana, Lothar Brecker, Mateja Pogorevc, Walter Steiner, Herfried Griengl, Thomas Kappe та Douglas W. Ribbons. "Proton-Nuclear Magnetic Resonance Analyses of the Substrate Specificity of a β-Ketolase from Pseudomonas putida, Acetopyruvate Hydrolase". Journal of Bacteriology 181, № 16 (15 серпня 1999): 5051–59. http://dx.doi.org/10.1128/jb.181.16.5051-5059.1999.
Повний текст джерелаHarcourt, Richard D., Karin Schaefer, and Michelle L. Coote. "Some Comments on Valence Bond Representations for the Radical Exchange Reaction X•+ R:Y → X:R + Y•." Journal of Physical Chemistry A 111, no. 50 (December 2007): 13278–82. http://dx.doi.org/10.1021/jp076864p.
Повний текст джерелаKondo, Michio, Kouji Okamoto, Ichiro Nishi, Makoto Yamamoto, Masood Jelokhani-Niaraki, and Hiroaki Kodama. "Hydrogen-Bond Detection in Peptides by1H-Nuclear Magnetic Resonance through a Hydrogen–Chlorine Exchange Reaction." Bulletin of the Chemical Society of Japan 67, no. 4 (April 1994): 1064–68. http://dx.doi.org/10.1246/bcsj.67.1064.
Повний текст джерела