Статті в журналах з теми "Homolysis"
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Zhang, Chen, Junxia Pi, Shu Chen, Ping Liu, and Peipei Sun. "Construction of a 4H-pyrido[4,3,2-gh]phenanthridin-5(6H)-one skeleton via a catalyst-free radical cascade addition/cyclization using azo compounds as radical sources." Organic Chemistry Frontiers 5, no. 5 (2018): 793–96. http://dx.doi.org/10.1039/c7qo00926g.
Повний текст джерелаShin, Jeongcheol, Jiseon Lee, Jong-Min Suh, and Kiyoung Park. "Ligand-field transition-induced C–S bond formation from nickelacycles." Chemical Science 12, no. 48 (2021): 15908–15. http://dx.doi.org/10.1039/d1sc05113j.
Повний текст джерелаQianzhu, Haocheng, Wenjuan Ji, Xinjian Ji, Leixia Chu, Chuchu Guo, Wei Lu, Wei Ding, Jiangtao Gao, and Qi Zhang. "Reactivity of the nitrogen-centered tryptophanyl radical in the catalysis by the radical SAM enzyme NosL." Chemical Communications 53, no. 2 (2017): 344–47. http://dx.doi.org/10.1039/c6cc08869d.
Повний текст джерелаIshihara, Koji, and Thomas Wilson Swaddle. "The pressure dependence of rates of homolytic fission of metal–ligand bonds in aqueous solution." Canadian Journal of Chemistry 64, no. 11 (November 1, 1986): 2168–70. http://dx.doi.org/10.1139/v86-356.
Повний текст джерелаYorimitsu, Hideki. "Homolytic substitution at phosphorus for C–P bond formation in organic synthesis." Beilstein Journal of Organic Chemistry 9 (June 28, 2013): 1269–77. http://dx.doi.org/10.3762/bjoc.9.143.
Повний текст джерелаCameron, Dale R., Alison M. P. Borrajo, Gregory R. J. Thatcher, and Brian M. Bennett. "Organic nitrates, thionitrates, peroxynitrites, and nitric oxide: a molecular orbital study of the (X = O, S) rearrangement, a reaction of potential biological significance." Canadian Journal of Chemistry 73, no. 10 (October 1, 1995): 1627–38. http://dx.doi.org/10.1139/v95-202.
Повний текст джерелаEdeleva, Mariya, Gerard Audran, Sylvain Marque, and Elena Bagryanskaya. "Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations." Materials 12, no. 5 (February 26, 2019): 688. http://dx.doi.org/10.3390/ma12050688.
Повний текст джерелаShu, Xing-Zhong, and Xiaobo Pang. "Titanium: A Unique Metal for Radical Dehydroxylative Functionalization of Alcohols." Synlett 32, no. 13 (March 4, 2021): 1269–74. http://dx.doi.org/10.1055/a-1406-0484.
Повний текст джерелаKoppenol, Willem H., and Reinhard Kissner. "Can ONOOH Undergo Homolysis?" Chemical Research in Toxicology 11, no. 2 (February 1998): 87–90. http://dx.doi.org/10.1021/tx970200x.
Повний текст джерелаTurrà, Natascia, Ulrich Neuenschwander, and Ive Hermans. "Molecule-Induced Peroxide Homolysis." ChemPhysChem 14, no. 8 (April 4, 2013): 1666–69. http://dx.doi.org/10.1002/cphc.201300130.
Повний текст джерелаMilne, Paul H., Danial D. M. Wayner, Dayal P. DeCosta, and James A. Pincock. "Substituent and charge distribution effects on the redox potentials of radicals. Thermodynamics for homolytic versus heterolytic cleavage in the 1-naphthylmethyl system." Canadian Journal of Chemistry 70, no. 1 (January 1, 1992): 121–27. http://dx.doi.org/10.1139/v92-021.
Повний текст джерелаGuselnikova, Olga, Gérard Audran, Jean-Patrick Joly, Andrii Trelin, Evgeny V. Tretyakov, Vaclav Svorcik, Oleksiy Lyutakov, Sylvain R. A. Marque, and Pavel Postnikov. "Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe." Chemical Science 12, no. 11 (2021): 4154–61. http://dx.doi.org/10.1039/d0sc06470j.
Повний текст джерелаSteffan, Carl R., James H. Espenson, and Andreja Bakac. "Oxidative homolysis of organochromium macrocycles." Inorganic Chemistry 30, no. 5 (March 1991): 1134–37. http://dx.doi.org/10.1021/ic00005a046.
Повний текст джерелаEdeleva, Mariya, Denis Morozov, Dmitriy Parkhomenko, Yulia Polienko, Anna Iurchenkova, Igor Kirilyuk, and Elena Bagryanskaya. "Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization." Chemical Communications 55, no. 2 (2019): 190–93. http://dx.doi.org/10.1039/c8cc08541b.
Повний текст джерелаChang, Mu-Chieh, Kate A. Jesse, Alexander S. Filatov, and John S. Anderson. "Reversible homolytic activation of water via metal–ligand cooperativity in a T-shaped Ni(ii) complex." Chemical Science 10, no. 5 (2019): 1360–67. http://dx.doi.org/10.1039/c8sc03719a.
Повний текст джерелаHUHTA, Marja S., Hao-Ping CHEN, Craig HEMANN, C. Russ HILLE, and E. Neil G. MARSH. "Protein–coenzyme interactions in adenosylcobalamin-dependent glutamate mutase." Biochemical Journal 355, no. 1 (February 26, 2001): 131–37. http://dx.doi.org/10.1042/bj3550131.
Повний текст джерелаSunada, Yusuke, Shintaro Ishida, Fumiya Hirakawa, Yoshihito Shiota, Kazunari Yoshizawa, Shinji Kanegawa, Osamu Sato, Hideo Nagashima та Takeaki Iwamoto. "Persistent four-coordinate iron-centered radical stabilized by π-donation". Chemical Science 7, № 1 (2016): 191–98. http://dx.doi.org/10.1039/c5sc02601f.
Повний текст джерелаZhang, Sheng Jian, and Ying Xian Zhao. "Kinetics and Selectivity of Cyclohexane Pyrolysis." Advanced Materials Research 455-456 (January 2012): 540–48. http://dx.doi.org/10.4028/www.scientific.net/amr.455-456.540.
Повний текст джерелаCherkasov, Sergey, Dmitriy Parkhomenko, Alexander Genaev, Georgii Salnikov, Mariya Edeleva, Denis Morozov, Tatyana Rybalova, Igor Kirilyuk, Sylvain R. A. Marque, and Elena Bagryanskaya. "NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines." Molecules 25, no. 21 (November 1, 2020): 5080. http://dx.doi.org/10.3390/molecules25215080.
Повний текст джерелаZhang, Ze Ping, Yan Lu, Min Zhi Rong, and Ming Qiu Zhang. "A thermally remendable and reprocessable crosslinked methyl methacrylate polymer based on oxygen insensitive dynamic reversible C–ON bonds." RSC Advances 6, no. 8 (2016): 6350–57. http://dx.doi.org/10.1039/c5ra22275c.
Повний текст джерелаZhao, Bo, Ju-You Lu, Yang Li, Dong-Huai Tu, Zhao-Tie Liu, Zhong-Wen Liu, and Jian Lu. "Regioisomerized atom transfer radical addition (ATRA) of olefins with dichlorofluorocarbons." RSC Advances 5, no. 123 (2015): 101412–15. http://dx.doi.org/10.1039/c5ra19244g.
Повний текст джерелаAudran, Gérard, Raphael Bikanga, Paul Brémond, Mariya Edeleva, Jean-Patrick Joly, Sylvain R. A. Marque, Paulin Nkolo, and Valérie Roubaud. "How intramolecular hydrogen bonding (IHB) controls the C–ON bond homolysis in alkoxyamines." Organic & Biomolecular Chemistry 15, no. 39 (2017): 8425–39. http://dx.doi.org/10.1039/c7ob02223a.
Повний текст джерелаLi, Hong Zhi, Lin Li, Zi Yan Zhong, Yi Han, LiHong Hu, and Ying Hua Lu. "An Accurate and Efficient Method to Predict Y-NO Bond Homolysis Bond Dissociation Energies." Mathematical Problems in Engineering 2013 (2013): 1–10. http://dx.doi.org/10.1155/2013/860357.
Повний текст джерелаZheng, Yue, Qian-Xiong Zhou, Yang-Yang Zhang, Chao Li, Yuan-Jun Hou, and Xue-Song Wang. "Substituent effect and wavelength dependence of the photoinduced Ru–O homolysis in the [Ru(bpy)2(py-SO3)]+-type complexes." Dalton Transactions 45, no. 7 (2016): 2897–905. http://dx.doi.org/10.1039/c5dt03694a.
Повний текст джерелаLi, Jun, Yang Yang, Ping Zhang, James R. Sounik, and Malcolm E. Kenney. "Synthesis, properties and drug potential of the photosensitive alkyl- and alkylsiloxy-ligated silicon phthalocyanine Pc 227." Photochem. Photobiol. Sci. 13, no. 12 (2014): 1690–98. http://dx.doi.org/10.1039/c4pp00321g.
Повний текст джерелаGong, Xianyun, Hongjun Kang, Yuyan Liu, and Songquan Wu. "Decomposition mechanisms and kinetics of amine/anhydride-cured DGEBA epoxy resin in near-critical water." RSC Advances 5, no. 50 (2015): 40269–82. http://dx.doi.org/10.1039/c5ra03828f.
Повний текст джерелаFokin, Andrey A., Boryslav A. Tkachenko, Oleg I. Korshunov, Pavel A. Gunchenko, and Peter R. Schreiner. "Molecule-Induced Alkane Homolysis with Dioxiranes." Journal of the American Chemical Society 123, no. 45 (November 2001): 11248–52. http://dx.doi.org/10.1021/ja0158096.
Повний текст джерелаSturzbecher-Höhne, Manuel, Thomas Nauser, Reinhard Kissner, and Willem H. Koppenol. "Photon-Initiated Homolysis of Peroxynitrous Acid." Inorganic Chemistry 48, no. 15 (August 3, 2009): 7307–12. http://dx.doi.org/10.1021/ic900614e.
Повний текст джерелаGaudel-Siri, Anouk, Didier Siri, and Paul Tordo. "Homolysis ofN-alkoxyamines: A Computational Study." ChemPhysChem 7, no. 2 (February 6, 2006): 430–38. http://dx.doi.org/10.1002/cphc.200500308.
Повний текст джерелаSong, Wenjing, and Andreja Bakac. "Oxidative Homolysis of a Nitrosylchromium Complex." Chemistry - A European Journal 14, no. 16 (May 29, 2008): 4906–12. http://dx.doi.org/10.1002/chem.200701750.
Повний текст джерелаAudran, Gerard, Matisse Batsiandzy Ibanou, Paul Brémond, Jean-Patrick Joly, and Sylvain R. A. Marque. "Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents." RSC Advances 5, no. 93 (2015): 76660–65. http://dx.doi.org/10.1039/c5ra13899j.
Повний текст джерелаKoirala, Agni Raj, Son Docao, and Kyung Byung Yoon. "Photocatalytic homolysis of methyl formate to dry formaldehyde on PdO/TiO2: photocatalytic reverse Tishchenko reaction of methyl formate." RSC Adv. 4, no. 63 (2014): 33144–48. http://dx.doi.org/10.1039/c4ra05744a.
Повний текст джерелаNkolo, Paulin, Gérard Audran, Raphael Bikanga, Paul Brémond, Sylvain R. A. Marque, and Valérie Roubaud. "C–ON bond homolysis of alkoxyamines: when too high polarity is detrimental." Organic & Biomolecular Chemistry 15, no. 29 (2017): 6167–76. http://dx.doi.org/10.1039/c7ob01312d.
Повний текст джерелаNesterova, Oksana V., Maxim L. Kuznetsov, Armando J. L. Pombeiro, Georgiy B. Shul'pin, and Dmytro S. Nesterov. "Homogeneous oxidation of C–H bonds with m-CPBA catalysed by a Co/Fe system: mechanistic insights from the point of view of the oxidant." Catalysis Science & Technology 12, no. 1 (2022): 282–99. http://dx.doi.org/10.1039/d1cy01991k.
Повний текст джерелаAudran, Gérard, Lionel Bosco, Paul Brémond, Natacha Jugniot, Sylvain R. A. Marque, Philippe Massot, Philippe Mellet, et al. "Enzymatic triggering of C–ON bond homolysis of alkoxyamines." Organic Chemistry Frontiers 6, no. 21 (2019): 3663–72. http://dx.doi.org/10.1039/c9qo00899c.
Повний текст джерелаAudran, Gérard, Elena Bagryanskaya, Irina Bagryanskaya, Mariya Edeleva, Jean-Patrick Joly, Sylvain R. A. Marque, Anna Iurchenkova, et al. "How intramolecular coordination bonding (ICB) controls the homolysis of the C–ON bond in alkoxyamines." RSC Advances 9, no. 44 (2019): 25776–89. http://dx.doi.org/10.1039/c9ra05334d.
Повний текст джерелаTorti, Edoardo, Gioia Della Giustina, Stefano Protti, Daniele Merli, Giovanna Brusatin, and Maurizio Fagnoni. "Aryl tosylates as non-ionic photoacid generators (PAGs): photochemistry and applications in cationic photopolymerizations." RSC Advances 5, no. 42 (2015): 33239–48. http://dx.doi.org/10.1039/c5ra03522h.
Повний текст джерелаAudran, Gérard, Elena Bagryanskaya, Irina Bagryanskaya, Paul Brémond, Mariya Edeleva, Sylvain R. A. Marque, Dmitriy Parkhomenko, Evgeny Tretyakov, and Svetlana Zhivetyeva. "C–ON bond homolysis of alkoxyamines triggered by paramagnetic copper(ii) salts." Inorganic Chemistry Frontiers 3, no. 11 (2016): 1464–72. http://dx.doi.org/10.1039/c6qi00277c.
Повний текст джерелаWilliams, G. K., and T. B. Brill. "Thermal Decomposition of Energetic Materials 70: Kinetics of Organic Peroxide Decomposition Derived from the Filament Control Voltage of T-Jump/FT-IR Spectroscopy." Applied Spectroscopy 51, no. 3 (March 1997): 423–27. http://dx.doi.org/10.1366/0003702971940314.
Повний текст джерелаPoli, Rinaldo. "A journey into metal–carbon bond homolysis." Comptes Rendus. Chimie 24, no. 1 (April 26, 2021): 147–75. http://dx.doi.org/10.5802/crchim.73.
Повний текст джерелаVenneri, Paul C., and John Warkentin. "Homolysis of Carbenes. Free Radicals from Dialkoxycarbenes." Journal of the American Chemical Society 120, no. 43 (November 1998): 11182–83. http://dx.doi.org/10.1021/ja982566h.
Повний текст джерелаBlau, Reed J., and James H. Espenson. "Homolysis and electron-transfer reactions of benzylcobalamin." Journal of the American Chemical Society 107, no. 12 (June 1985): 3530–33. http://dx.doi.org/10.1021/ja00298a021.
Повний текст джерелаKelley, Douglas G., Adam Marchaj, Andreja Bakac, and James H. Espenson. "Formation and homolysis of organonickel(III) complexes." Journal of the American Chemical Society 113, no. 20 (September 1991): 7583–87. http://dx.doi.org/10.1021/ja00020a020.
Повний текст джерелаZhulin, V. M., T. V. Lipovich, and V. L. Antonovskii. "Homolysis of dicyclohexyl peroxydicarbonate at various pressures." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 7 (July 1988): 1338–42. http://dx.doi.org/10.1007/bf00962735.
Повний текст джерелаBakac, Andreja, James H. Espenson, and James A. Janni. "Oxidative homolysis of the superoxopentaaquachromium(III)ion." Journal of the Chemical Society, Chemical Communications, no. 3 (1994): 315. http://dx.doi.org/10.1039/c39940000315.
Повний текст джерелаBeaudoin, Emmanuel, Denis Bertin, Didier Gigmes, Sylvain R. A. Marque, Didier Siri, and Paul Tordo. "Alkoxyamine C–ON Bond Homolysis: Stereoelectronic Effects." European Journal of Organic Chemistry 2006, no. 7 (April 2006): 1755–68. http://dx.doi.org/10.1002/ejoc.200500725.
Повний текст джерелаSandhiya, Lakshmanan, and Hendrik Zipse. "OO bond homolysis in hydrogen peroxide." Journal of Computational Chemistry 38, no. 25 (July 11, 2017): 2186–92. http://dx.doi.org/10.1002/jcc.24870.
Повний текст джерелаSana, Michel, Georges Leroy, Jean-Luc Vaerman, and Heinz Gunter Viehe. "The thermal isomerization of bicyclic oxazines into epoxyepimines. A preliminary theoretical study." Canadian Journal of Chemistry 68, no. 9 (September 1, 1990): 1625–28. http://dx.doi.org/10.1139/v90-251.
Повний текст джерелаDöpp, Dietrich. "The surprising photochemistry of sultams related to saccharin." International Journal of Photoenergy 3, no. 1 (2001): 41–48. http://dx.doi.org/10.1155/s1110662x01000058.
Повний текст джерелаLi, S., та K. Lundquist. "Reactions of the β-Aryl Ether Lignin Model 1-(4-Hydroxy-3-Methoxyphenyl)-2-(2-Methoxyphenoxy)-1-Propanol on Heating in Aqueous Solution". Holzforschung 55, № 3 (25 квітня 2001): 296–301. http://dx.doi.org/10.1515/hf.2001.049.
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