Статті в журналах з теми "Homolytic cleavage of diborons"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Homolytic cleavage of diborons".
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.
Verma, Piyush Kumar, Naresh Kumar Meher, and K. Geetharani. "Homolytic cleavage of diboron(4) compounds using diazabutadiene derivatives." Chemical Communications 57, no. 64 (2021): 7886–89. http://dx.doi.org/10.1039/d1cc02881b.
Повний текст джерелаWang, Pengfei, Yuli Li, and Guangwei Wang. "Tetrahydroxydiboron-Initiated Atom-Transfer Radical Cyclization." Synthesis 53, no. 19 (April 19, 2021): 3555–63. http://dx.doi.org/10.1055/a-1485-4956.
Повний текст джерелаCao, Levy L., and Douglas W. Stephan. "Homolytic Cleavage Reactions of a Neutral Doubly Base Stabilized Diborane(4)." Organometallics 36, no. 16 (August 9, 2017): 3163–70. http://dx.doi.org/10.1021/acs.organomet.7b00522.
Повний текст джерелаWang, Jiaoyang, Wenrui Zheng, and Yuanyuan Zheng. "Theoretical study on homolytic B–B cleavages of diboron(4) compounds." RSC Adv. 7, no. 78 (2017): 49251–72. http://dx.doi.org/10.1039/c7ra09006d.
Повний текст джерелаTsurugi, Hayato, Kazushi Mashima, Luis C. Misal Castro, and Ibrahim Sultan. "Pyridine-Mediated B–B Bond Activation of (RO)2B–B(OR)2 for Generating Borylpyridine Anions and Pyridine-Stabilized Boryl Radicals as Useful Boryl Reagents in Organic Synthesis." Synthesis 53, no. 18 (April 20, 2021): 3211–26. http://dx.doi.org/10.1055/a-1486-8169.
Повний текст джерелаWeng, Zhiqiang, and Lai Yoong Goh. "Homolytic Cleavage and Aggregation Processes in Cyclopentadienylchromium Chemistry." Accounts of Chemical Research 37, no. 3 (March 2004): 187–99. http://dx.doi.org/10.1021/ar030003r.
Повний текст джерелаDing, Lanlan, Wenrui Zheng, and Yingxing Wang. "Homolytic C–O Cleavage in Phosphates and Sulfonates." Journal of Physical Chemistry A 119, no. 14 (March 27, 2015): 3488–99. http://dx.doi.org/10.1021/acs.jpca.5b00569.
Повний текст джерелаKampmeier, Jack A. "Regioselectivity in the Homolytic Cleavage of S-Adenosylmethionine." Biochemistry 49, no. 51 (December 28, 2010): 10770–72. http://dx.doi.org/10.1021/bi101509u.
Повний текст джерелаNome, Faruk, Marcos Caroli Rezende, Claudia Maria Sabóia, and Arlindo Clemente Da Silva. "Kinetics of the thermolysis of para-substituted benzylcobalamins and derivatives." Canadian Journal of Chemistry 65, no. 9 (September 1, 1987): 2095–99. http://dx.doi.org/10.1139/v87-347.
Повний текст джерелаBajaj, Ashima, Rishu Khurana, and Md Ehesan Ali. "Quantum interference and spin filtering effects in photo-responsive single molecule devices." Journal of Materials Chemistry C 9, no. 34 (2021): 11242–51. http://dx.doi.org/10.1039/d1tc02200h.
Повний текст джерелаLi, Yan, Kartik Chandra Mondal, Peter Stollberg, Hongping Zhu, Herbert W. Roesky, Regine Herbst-Irmer, Dietmar Stalke, and Heike Fliegl. "Unusual formation of a N-heterocyclic germylene via homolytic cleavage of a C–C bond." Chem. Commun. 50, no. 25 (2014): 3356–58. http://dx.doi.org/10.1039/c4cc00251b.
Повний текст джерелаSiegel, Marshall M., and Norman B. Colthup. "Molecular Orbital Study of Remote Charge Site Decompositions in the Collision-Induced Decomposition Mass Spectra of Fatty Acid Carboxylate Anions." Applied Spectroscopy 42, no. 7 (September 1988): 1214–21. http://dx.doi.org/10.1366/0003702884429887.
Повний текст джерелаHosseini, Seyedeh Nargess, Jeffrey R. Johnston, and F. G. West. "Evidence for heterolytic cleavage of a cyclic oxonium ylide: implications for the mechanism of the Stevens [1,2]-shift." Chemical Communications 53, no. 94 (2017): 12654–56. http://dx.doi.org/10.1039/c7cc07716e.
Повний текст джерелаHou, Bo, David Benito-Alifonso, Richard Webster, David Cherns, M. Carmen Galan, and David J. Fermín. "Rapid phosphine-free synthesis of CdSe quantum dots: promoting the generation of Se precursors using a radical initiator." J. Mater. Chem. A 2, no. 19 (2014): 6879–86. http://dx.doi.org/10.1039/c4ta00285g.
Повний текст джерелаAndrieux, C. P., F. Gonzalez, and J. M. Savéant. "Homolytic and heterolytic radical cleavage in the Kolbe reaction." Journal of Electroanalytical Chemistry 498, no. 1-2 (February 2001): 171–80. http://dx.doi.org/10.1016/s0022-0728(00)00365-x.
Повний текст джерелаHill, Nicholas S., Melinda J. Fule, Jason Morris, Jean-Louis Clément, Yohann Guillaneuf, Didier Gigmes, and Michelle L. Coote. "Mesolytic Versus Homolytic Cleavage in Photochemical Nitroxide-Mediated Polymerization." Macromolecules 53, no. 5 (February 26, 2020): 1567–72. http://dx.doi.org/10.1021/acs.macromol.0c00134.
Повний текст джерелаArnett, Edward M., Sampath Venimadhavan, and Kalyani Amarnath. "Homolytic and heterolytic cleavage energies for carbon-nitrogen bonds." Journal of the American Chemical Society 114, no. 14 (July 1992): 5598–602. http://dx.doi.org/10.1021/ja00040a018.
Повний текст джерелаLIU, MIN HSIEN, and GEN FA ZHENG. "COMPUTATIONAL STUDY OF UNIMOLECULAR DECOMPOSITION MECHANISM OF RDX EXPLOSIVE." Journal of Theoretical and Computational Chemistry 06, no. 02 (June 2007): 341–51. http://dx.doi.org/10.1142/s0219633607002952.
Повний текст джерелаMondol, Ranajit, and Edwin Otten. "Structure and bonding in reduced boron and aluminium complexes with formazanate ligands." Dalton Transactions 48, no. 37 (2019): 13981–88. http://dx.doi.org/10.1039/c9dt02831e.
Повний текст джерелаWard, Antony J., Rebecca A. Lesic, Nicholas Proschogo, Anthony F. Masters, and Thomas Maschmeyer. "Strained surface siloxanes as a source of synthetically important radicals." RSC Advances 5, no. 122 (2015): 100618–24. http://dx.doi.org/10.1039/c5ra20399f.
Повний текст джерелаFoster, B., B. Gaillard, N. Mathur, A. L. Pincock, J. A. Pincock, and C. Sehmbey. "Substituent effects on homolytic versus heterolytic photocleavage of (1-naphthylmethyl)trimethylammonium chlorides." Canadian Journal of Chemistry 65, no. 7 (July 1, 1987): 1599–607. http://dx.doi.org/10.1139/v87-268.
Повний текст джерелаIguchi, Daniela, Rosa Erra-Balsells, and Sergio M. Bonesi. "Photo-Fries rearrangement of aryl acetamides: regioselectivity induced by the aqueous micellar green environment." Photochemical & Photobiological Sciences 15, no. 1 (2016): 105–16. http://dx.doi.org/10.1039/c5pp00349k.
Повний текст джерелаZheng, Yue, Qianxiong Zhou, Wanhua Lei, Yuanjun Hou, Ke Li, Yongjie Chen, Baowen Zhang, and Xuesong Wang. "DNA photocleavage in anaerobic conditions by a Ru(ii) complex: a new mechanism." Chemical Communications 51, no. 2 (2015): 428–30. http://dx.doi.org/10.1039/c4cc06552b.
Повний текст джерелаArnold, B., L. Donald, A. Jurgens, and J. A. Pincock. "Homolytic versus heterolytic cleavage for the photochemistry of 1-naphthylmethyl derivatives." Canadian Journal of Chemistry 63, no. 11 (November 1, 1985): 3140–46. http://dx.doi.org/10.1139/v85-518.
Повний текст джерелаLi, Jing, Martin J. Lear та Yujiro Hayashi. "Autoinductive conversion of α,α-diiodonitroalkanes to amides and esters catalysed by iodine byproducts under O2". Chemical Communications 54, № 49 (2018): 6360–63. http://dx.doi.org/10.1039/c8cc03191f.
Повний текст джерелаKlepel, Florian, and Bart Jan Ravoo. "Dynamic covalent chemistry in aqueous solution by photoinduced radical disulfide metathesis." Organic & Biomolecular Chemistry 15, no. 18 (2017): 3840–42. http://dx.doi.org/10.1039/c7ob00667e.
Повний текст джерелаRagnar, Martin, Tord Eriksson, Torbjörn Reitberger, and Peter Brandt. "A New Mechanism in the Ozone Reaction with Lignin Like Structures." Holzforschung 53, no. 4 (July 1, 1999): 423–28. http://dx.doi.org/10.1515/hf.1999.070.
Повний текст джерелаJi, Yu, Qiang Yao, Yueying Zhao, and Weihong Cao. "On the Origin of Alkali-Catalyzed Aromatization of Phenols." Polymers 11, no. 7 (July 2, 2019): 1119. http://dx.doi.org/10.3390/polym11071119.
Повний текст джерелаMallorquin, Rocio Martinez, Guillaume Vincent, Etienne Derat, Max Malacria, Jean-Philippe Goddard, and Louis Fensterbank. "New Elements on the Behaviour of a Bissulfinylmethyl Radical." Australian Journal of Chemistry 66, no. 3 (2013): 346. http://dx.doi.org/10.1071/ch12545.
Повний текст джерелаBracker, Mario, Lucas Helmecke, Martin Kleinschmidt, Constantin Czekelius, and Christel M. Marian. "Visible Light-Induced Homolytic Cleavage of Perfluoroalkyl Iodides Mediated by Phosphines." Molecules 25, no. 7 (April 1, 2020): 1606. http://dx.doi.org/10.3390/molecules25071606.
Повний текст джерелаCostentin, Cyrille, Marc Robert, and Jean-Michel Savéant. "Activation Barriers in the Homolytic Cleavage of Radicals and Ion Radicals." Journal of the American Chemical Society 125, no. 1 (January 2003): 105–12. http://dx.doi.org/10.1021/ja027287f.
Повний текст джерелаVagánek, Adam, Ján Rimarčík, Michal Ilčin, Peter Škorňa, Vladimír Lukeš, and Erik Klein. "Homolytic N–H bond cleavage in anilines: Energetics and substituent effect." Computational and Theoretical Chemistry 1014 (June 2013): 60–67. http://dx.doi.org/10.1016/j.comptc.2013.03.027.
Повний текст джерелаLEVITIN, J. YA, A. K. YATSIMIRSKII, and M. E. VOL'PIN. "ChemInform Abstract: Mechanisms of the Homolytic Cleavage of Organo-Cobalt Complexes." ChemInform 22, no. 18 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199118312.
Повний текст джерелаArantes, Guilherme M., Anirban Bhattacharjee, and Martin J. Field. "Homolytic Cleavage of FeS Bonds in Rubredoxin under Mechanical Stress." Angewandte Chemie 125, no. 31 (June 18, 2013): 8302–4. http://dx.doi.org/10.1002/ange.201303462.
Повний текст джерелаArantes, Guilherme M., Anirban Bhattacharjee, and Martin J. Field. "Homolytic Cleavage of FeS Bonds in Rubredoxin under Mechanical Stress." Angewandte Chemie International Edition 52, no. 31 (June 18, 2013): 8144–46. http://dx.doi.org/10.1002/anie.201303462.
Повний текст джерелаMorrow, GR, and ID Rae. "Thermal-Degradation of Polymers and Polymer Models. IV. Thermolysis of a Polymethacrylate Model With an Unsaturated End Group." Australian Journal of Chemistry 40, no. 8 (1987): 1477. http://dx.doi.org/10.1071/ch9871477.
Повний текст джерелаBen Amor, N., and C. Daniel. "Spin–orbit ab initio investigation of the UV photoinduced bond cleavage in iodotrimethylstannane." Canadian Journal of Chemistry 87, no. 7 (July 2009): 1006–12. http://dx.doi.org/10.1139/v09-064.
Повний текст джерелаDing, Lanlan, Wenrui Zheng, and Yingxing Wang. "Theoretical study on homolytic C(sp2)–O cleavage in ethers and phenols." New Journal of Chemistry 39, no. 9 (2015): 6935–43. http://dx.doi.org/10.1039/c5nj01354b.
Повний текст джерелаBarroso, J., A. R. Pierna, T. C. Blanco, E. Morallón, and F. Huerta. "Homolytic cleavage C–C bond in the electrooxidation of ethanol and bioethanol." Journal of Power Sources 196, no. 9 (May 2011): 4193–99. http://dx.doi.org/10.1016/j.jpowsour.2010.09.087.
Повний текст джерелаGroves, John T., and Yoshihito Watanabe. "Heterolytic and homolytic oxygen-oxygen bond cleavage reactions of acylperoxomanganese(III) porphyrins." Inorganic Chemistry 25, no. 27 (December 1986): 4808–10. http://dx.doi.org/10.1021/ic00247a006.
Повний текст джерелаVagánek, Adam, Ján Rimarčík, Vladimír Lukeš, and Erik Klein. "On the energetics of homolytic and heterolytic OH bond cleavage in flavonoids." Computational and Theoretical Chemistry 991 (July 2012): 192–200. http://dx.doi.org/10.1016/j.comptc.2012.04.014.
Повний текст джерелаMurphy, Barry E., Sergey A. Krasnikov, Natalia N. Sergeeva, Attilio A. Cafolla, Alexei B. Preobrajenski, Alexander N. Chaika, Olaf Lübben, and Igor V. Shvets. "Homolytic Cleavage of Molecular Oxygen by Manganese Porphyrins Supported on Ag(111)." ACS Nano 8, no. 5 (April 30, 2014): 5190–98. http://dx.doi.org/10.1021/nn501240j.
Повний текст джерелаGansäuer, Andreas, Björn Rinker, Marianna Pierobon, Stefan Grimme, Mareike Gerenkamp, and Christian Mück-Lichtenfeld. "A Radical Tandem Reaction with Homolytic Cleavage of a TiO Bond." Angewandte Chemie International Edition 42, no. 31 (August 11, 2003): 3687–90. http://dx.doi.org/10.1002/anie.200351240.
Повний текст джерелаZheng, Wenrui, Lanlan Ding, Jiaoyang Wang, and Yingxing Wang. "Computational study on alkenyl/aryl C(sp2)–O homolytic cleavage of carboxylates and carbamates." RSC Advances 6, no. 32 (2016): 26514–25. http://dx.doi.org/10.1039/c5ra27859g.
Повний текст джерелаWang, Lele, Wenzhao Qiu, Hongge Shao, and Rusheng Yuan. "Photoinduced C-C Cross-Coupling of Aryl Chlorides and Inert Arenes." International Journal of Photoenergy 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/5632613.
Повний текст джерелаPaul, Ganesh Chandra, Samir Ghorai, and Chandan Mukherjee. "Monoradical-containing four-coordinate Co(iii) complexes: homolytic S–S and Se–Se bond cleavage and catalytic isocyanate to urea conversion under sunlight." Chemical Communications 53, no. 57 (2017): 8022–25. http://dx.doi.org/10.1039/c7cc03486e.
Повний текст джерелаDohi, Toshifumi, Shohei Ueda, Kosuke Iwasaki, Yusuke Tsunoda, Koji Morimoto, and Yasuyuki Kita. "Selective carboxylation of reactive benzylic C–H bonds by a hypervalent iodine(III)/inorganic bromide oxidation system." Beilstein Journal of Organic Chemistry 14 (May 16, 2018): 1087–94. http://dx.doi.org/10.3762/bjoc.14.94.
Повний текст джерелаLesimple, Alain, Yves Le Bigot, Michel Delmas, and Joseph Banoub. "Electron ionization mass spectrometry of difurfuryl diamines." Spectroscopy 14, no. 3 (2000): 109–14. http://dx.doi.org/10.1155/2000/453723.
Повний текст джерелаGunawardhana, Nanda, and Stephen L. Gipson. "Reductively induced homolytic carbon–carbon bond cleavage in Co(CO)3(PPh3)(COCF3)." Journal of Organometallic Chemistry 692, no. 15 (July 2007): 3231–35. http://dx.doi.org/10.1016/j.jorganchem.2006.12.027.
Повний текст джерелаAllentoff, Alban J., Judy L. Bolton, Angela Wilks, John A. Thompson, and Paul R. Ortiz de Montellano. "Heterolytic versus homolytic peroxide bond cleavage by sperm whale myoglobin and myoglobin mutants." Journal of the American Chemical Society 114, no. 25 (December 1992): 9744–49. http://dx.doi.org/10.1021/ja00051a003.
Повний текст джерела