Artigos de revistas sobre o tema "Homolysis"
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Zhang, Chen, Junxia Pi, Shu Chen, Ping Liu e 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, n.º 5 (2018): 793–96. http://dx.doi.org/10.1039/c7qo00926g.
Texto completo da fonteShin, Jeongcheol, Jiseon Lee, Jong-Min Suh e Kiyoung Park. "Ligand-field transition-induced C–S bond formation from nickelacycles". Chemical Science 12, n.º 48 (2021): 15908–15. http://dx.doi.org/10.1039/d1sc05113j.
Texto completo da fonteQianzhu, Haocheng, Wenjuan Ji, Xinjian Ji, Leixia Chu, Chuchu Guo, Wei Lu, Wei Ding, Jiangtao Gao e Qi Zhang. "Reactivity of the nitrogen-centered tryptophanyl radical in the catalysis by the radical SAM enzyme NosL". Chemical Communications 53, n.º 2 (2017): 344–47. http://dx.doi.org/10.1039/c6cc08869d.
Texto completo da fonteIshihara, Koji, e Thomas Wilson Swaddle. "The pressure dependence of rates of homolytic fission of metal–ligand bonds in aqueous solution". Canadian Journal of Chemistry 64, n.º 11 (1 de novembro de 1986): 2168–70. http://dx.doi.org/10.1139/v86-356.
Texto completo da fonteYorimitsu, Hideki. "Homolytic substitution at phosphorus for C–P bond formation in organic synthesis". Beilstein Journal of Organic Chemistry 9 (28 de junho de 2013): 1269–77. http://dx.doi.org/10.3762/bjoc.9.143.
Texto completo da fonteCameron, Dale R., Alison M. P. Borrajo, Gregory R. J. Thatcher e 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, n.º 10 (1 de outubro de 1995): 1627–38. http://dx.doi.org/10.1139/v95-202.
Texto completo da fonteEdeleva, Mariya, Gerard Audran, Sylvain Marque e Elena Bagryanskaya. "Smart Control of Nitroxide-Mediated Polymerization Initiators’ Reactivity by pH, Complexation with Metals, and Chemical Transformations". Materials 12, n.º 5 (26 de fevereiro de 2019): 688. http://dx.doi.org/10.3390/ma12050688.
Texto completo da fonteShu, Xing-Zhong, e Xiaobo Pang. "Titanium: A Unique Metal for Radical Dehydroxylative Functionalization of Alcohols". Synlett 32, n.º 13 (4 de março de 2021): 1269–74. http://dx.doi.org/10.1055/a-1406-0484.
Texto completo da fonteKoppenol, Willem H., e Reinhard Kissner. "Can ONOOH Undergo Homolysis?" Chemical Research in Toxicology 11, n.º 2 (fevereiro de 1998): 87–90. http://dx.doi.org/10.1021/tx970200x.
Texto completo da fonteTurrà, Natascia, Ulrich Neuenschwander e Ive Hermans. "Molecule-Induced Peroxide Homolysis". ChemPhysChem 14, n.º 8 (4 de abril de 2013): 1666–69. http://dx.doi.org/10.1002/cphc.201300130.
Texto completo da fonteMilne, Paul H., Danial D. M. Wayner, Dayal P. DeCosta e 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, n.º 1 (1 de janeiro de 1992): 121–27. http://dx.doi.org/10.1139/v92-021.
Texto completo da fonteGuselnikova, Olga, Gérard Audran, Jean-Patrick Joly, Andrii Trelin, Evgeny V. Tretyakov, Vaclav Svorcik, Oleksiy Lyutakov, Sylvain R. A. Marque e Pavel Postnikov. "Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe". Chemical Science 12, n.º 11 (2021): 4154–61. http://dx.doi.org/10.1039/d0sc06470j.
Texto completo da fonteSteffan, Carl R., James H. Espenson e Andreja Bakac. "Oxidative homolysis of organochromium macrocycles". Inorganic Chemistry 30, n.º 5 (março de 1991): 1134–37. http://dx.doi.org/10.1021/ic00005a046.
Texto completo da fonteEdeleva, Mariya, Denis Morozov, Dmitriy Parkhomenko, Yulia Polienko, Anna Iurchenkova, Igor Kirilyuk e Elena Bagryanskaya. "Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization". Chemical Communications 55, n.º 2 (2019): 190–93. http://dx.doi.org/10.1039/c8cc08541b.
Texto completo da fonteChang, Mu-Chieh, Kate A. Jesse, Alexander S. Filatov e John S. Anderson. "Reversible homolytic activation of water via metal–ligand cooperativity in a T-shaped Ni(ii) complex". Chemical Science 10, n.º 5 (2019): 1360–67. http://dx.doi.org/10.1039/c8sc03719a.
Texto completo da fonteHUHTA, Marja S., Hao-Ping CHEN, Craig HEMANN, C. Russ HILLE e E. Neil G. MARSH. "Protein–coenzyme interactions in adenosylcobalamin-dependent glutamate mutase". Biochemical Journal 355, n.º 1 (26 de fevereiro de 2001): 131–37. http://dx.doi.org/10.1042/bj3550131.
Texto completo da fonteSunada, Yusuke, Shintaro Ishida, Fumiya Hirakawa, Yoshihito Shiota, Kazunari Yoshizawa, Shinji Kanegawa, Osamu Sato, Hideo Nagashima e Takeaki Iwamoto. "Persistent four-coordinate iron-centered radical stabilized by π-donation". Chemical Science 7, n.º 1 (2016): 191–98. http://dx.doi.org/10.1039/c5sc02601f.
Texto completo da fonteZhang, Sheng Jian, e Ying Xian Zhao. "Kinetics and Selectivity of Cyclohexane Pyrolysis". Advanced Materials Research 455-456 (janeiro de 2012): 540–48. http://dx.doi.org/10.4028/www.scientific.net/amr.455-456.540.
Texto completo da fonteCherkasov, Sergey, Dmitriy Parkhomenko, Alexander Genaev, Georgii Salnikov, Mariya Edeleva, Denis Morozov, Tatyana Rybalova, Igor Kirilyuk, Sylvain R. A. Marque e Elena Bagryanskaya. "NMR and EPR Study of Homolysis of Diastereomeric Alkoxyamines". Molecules 25, n.º 21 (1 de novembro de 2020): 5080. http://dx.doi.org/10.3390/molecules25215080.
Texto completo da fonteZhang, Ze Ping, Yan Lu, Min Zhi Rong e Ming Qiu Zhang. "A thermally remendable and reprocessable crosslinked methyl methacrylate polymer based on oxygen insensitive dynamic reversible C–ON bonds". RSC Advances 6, n.º 8 (2016): 6350–57. http://dx.doi.org/10.1039/c5ra22275c.
Texto completo da fonteZhao, Bo, Ju-You Lu, Yang Li, Dong-Huai Tu, Zhao-Tie Liu, Zhong-Wen Liu e Jian Lu. "Regioisomerized atom transfer radical addition (ATRA) of olefins with dichlorofluorocarbons". RSC Advances 5, n.º 123 (2015): 101412–15. http://dx.doi.org/10.1039/c5ra19244g.
Texto completo da fonteAudran, Gérard, Raphael Bikanga, Paul Brémond, Mariya Edeleva, Jean-Patrick Joly, Sylvain R. A. Marque, Paulin Nkolo e Valérie Roubaud. "How intramolecular hydrogen bonding (IHB) controls the C–ON bond homolysis in alkoxyamines". Organic & Biomolecular Chemistry 15, n.º 39 (2017): 8425–39. http://dx.doi.org/10.1039/c7ob02223a.
Texto completo da fonteLi, Hong Zhi, Lin Li, Zi Yan Zhong, Yi Han, LiHong Hu e 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.
Texto completo da fonteZheng, Yue, Qian-Xiong Zhou, Yang-Yang Zhang, Chao Li, Yuan-Jun Hou e 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, n.º 7 (2016): 2897–905. http://dx.doi.org/10.1039/c5dt03694a.
Texto completo da fonteLi, Jun, Yang Yang, Ping Zhang, James R. Sounik e Malcolm E. Kenney. "Synthesis, properties and drug potential of the photosensitive alkyl- and alkylsiloxy-ligated silicon phthalocyanine Pc 227". Photochem. Photobiol. Sci. 13, n.º 12 (2014): 1690–98. http://dx.doi.org/10.1039/c4pp00321g.
Texto completo da fonteGong, Xianyun, Hongjun Kang, Yuyan Liu e Songquan Wu. "Decomposition mechanisms and kinetics of amine/anhydride-cured DGEBA epoxy resin in near-critical water". RSC Advances 5, n.º 50 (2015): 40269–82. http://dx.doi.org/10.1039/c5ra03828f.
Texto completo da fonteFokin, Andrey A., Boryslav A. Tkachenko, Oleg I. Korshunov, Pavel A. Gunchenko e Peter R. Schreiner. "Molecule-Induced Alkane Homolysis with Dioxiranes". Journal of the American Chemical Society 123, n.º 45 (novembro de 2001): 11248–52. http://dx.doi.org/10.1021/ja0158096.
Texto completo da fonteSturzbecher-Höhne, Manuel, Thomas Nauser, Reinhard Kissner e Willem H. Koppenol. "Photon-Initiated Homolysis of Peroxynitrous Acid". Inorganic Chemistry 48, n.º 15 (3 de agosto de 2009): 7307–12. http://dx.doi.org/10.1021/ic900614e.
Texto completo da fonteGaudel-Siri, Anouk, Didier Siri e Paul Tordo. "Homolysis ofN-alkoxyamines: A Computational Study". ChemPhysChem 7, n.º 2 (6 de fevereiro de 2006): 430–38. http://dx.doi.org/10.1002/cphc.200500308.
Texto completo da fonteSong, Wenjing, e Andreja Bakac. "Oxidative Homolysis of a Nitrosylchromium Complex". Chemistry - A European Journal 14, n.º 16 (29 de maio de 2008): 4906–12. http://dx.doi.org/10.1002/chem.200701750.
Texto completo da fonteAudran, Gerard, Matisse Batsiandzy Ibanou, Paul Brémond, Jean-Patrick Joly e Sylvain R. A. Marque. "Part 10: chemically triggered alkoxyamine C–ON bond homolysis in ionic liquid solvents". RSC Advances 5, n.º 93 (2015): 76660–65. http://dx.doi.org/10.1039/c5ra13899j.
Texto completo da fonteKoirala, Agni Raj, Son Docao e Kyung Byung Yoon. "Photocatalytic homolysis of methyl formate to dry formaldehyde on PdO/TiO2: photocatalytic reverse Tishchenko reaction of methyl formate". RSC Adv. 4, n.º 63 (2014): 33144–48. http://dx.doi.org/10.1039/c4ra05744a.
Texto completo da fonteNkolo, Paulin, Gérard Audran, Raphael Bikanga, Paul Brémond, Sylvain R. A. Marque e Valérie Roubaud. "C–ON bond homolysis of alkoxyamines: when too high polarity is detrimental". Organic & Biomolecular Chemistry 15, n.º 29 (2017): 6167–76. http://dx.doi.org/10.1039/c7ob01312d.
Texto completo da fonteNesterova, Oksana V., Maxim L. Kuznetsov, Armando J. L. Pombeiro, Georgiy B. Shul'pin e 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, n.º 1 (2022): 282–99. http://dx.doi.org/10.1039/d1cy01991k.
Texto completo da fonteAudran, 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, n.º 21 (2019): 3663–72. http://dx.doi.org/10.1039/c9qo00899c.
Texto completo da fonteAudran, 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, n.º 44 (2019): 25776–89. http://dx.doi.org/10.1039/c9ra05334d.
Texto completo da fonteTorti, Edoardo, Gioia Della Giustina, Stefano Protti, Daniele Merli, Giovanna Brusatin e Maurizio Fagnoni. "Aryl tosylates as non-ionic photoacid generators (PAGs): photochemistry and applications in cationic photopolymerizations". RSC Advances 5, n.º 42 (2015): 33239–48. http://dx.doi.org/10.1039/c5ra03522h.
Texto completo da fonteAudran, Gérard, Elena Bagryanskaya, Irina Bagryanskaya, Paul Brémond, Mariya Edeleva, Sylvain R. A. Marque, Dmitriy Parkhomenko, Evgeny Tretyakov e Svetlana Zhivetyeva. "C–ON bond homolysis of alkoxyamines triggered by paramagnetic copper(ii) salts". Inorganic Chemistry Frontiers 3, n.º 11 (2016): 1464–72. http://dx.doi.org/10.1039/c6qi00277c.
Texto completo da fonteWilliams, G. K., e 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, n.º 3 (março de 1997): 423–27. http://dx.doi.org/10.1366/0003702971940314.
Texto completo da fontePoli, Rinaldo. "A journey into metal–carbon bond homolysis". Comptes Rendus. Chimie 24, n.º 1 (26 de abril de 2021): 147–75. http://dx.doi.org/10.5802/crchim.73.
Texto completo da fonteVenneri, Paul C., e John Warkentin. "Homolysis of Carbenes. Free Radicals from Dialkoxycarbenes". Journal of the American Chemical Society 120, n.º 43 (novembro de 1998): 11182–83. http://dx.doi.org/10.1021/ja982566h.
Texto completo da fonteBlau, Reed J., e James H. Espenson. "Homolysis and electron-transfer reactions of benzylcobalamin". Journal of the American Chemical Society 107, n.º 12 (junho de 1985): 3530–33. http://dx.doi.org/10.1021/ja00298a021.
Texto completo da fonteKelley, Douglas G., Adam Marchaj, Andreja Bakac e James H. Espenson. "Formation and homolysis of organonickel(III) complexes". Journal of the American Chemical Society 113, n.º 20 (setembro de 1991): 7583–87. http://dx.doi.org/10.1021/ja00020a020.
Texto completo da fonteZhulin, V. M., T. V. Lipovich e V. L. Antonovskii. "Homolysis of dicyclohexyl peroxydicarbonate at various pressures". Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, n.º 7 (julho de 1988): 1338–42. http://dx.doi.org/10.1007/bf00962735.
Texto completo da fonteBakac, Andreja, James H. Espenson e James A. Janni. "Oxidative homolysis of the superoxopentaaquachromium(III)ion". Journal of the Chemical Society, Chemical Communications, n.º 3 (1994): 315. http://dx.doi.org/10.1039/c39940000315.
Texto completo da fonteBeaudoin, Emmanuel, Denis Bertin, Didier Gigmes, Sylvain R. A. Marque, Didier Siri e Paul Tordo. "Alkoxyamine C–ON Bond Homolysis: Stereoelectronic Effects". European Journal of Organic Chemistry 2006, n.º 7 (abril de 2006): 1755–68. http://dx.doi.org/10.1002/ejoc.200500725.
Texto completo da fonteSandhiya, Lakshmanan, e Hendrik Zipse. "OO bond homolysis in hydrogen peroxide". Journal of Computational Chemistry 38, n.º 25 (11 de julho de 2017): 2186–92. http://dx.doi.org/10.1002/jcc.24870.
Texto completo da fonteSana, Michel, Georges Leroy, Jean-Luc Vaerman e Heinz Gunter Viehe. "The thermal isomerization of bicyclic oxazines into epoxyepimines. A preliminary theoretical study". Canadian Journal of Chemistry 68, n.º 9 (1 de setembro de 1990): 1625–28. http://dx.doi.org/10.1139/v90-251.
Texto completo da fonteDöpp, Dietrich. "The surprising photochemistry of sultams related to saccharin". International Journal of Photoenergy 3, n.º 1 (2001): 41–48. http://dx.doi.org/10.1155/s1110662x01000058.
Texto completo da fonteLi, S., e 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, n.º 3 (25 de abril de 2001): 296–301. http://dx.doi.org/10.1515/hf.2001.049.
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