Synthesis and Structure of Tetraphenylantimony Methacrylate and Tetraphenylantimony Crotonate and Their Use for the Production of Antimony-Containing Polystyrene
Tetraphenylantimony methacrylate Ph 4 SbO 2 CC(CH 3 )=CH 2 and tetraphenylantimony crotonate Ph 4 SbO 2 CCH=CHCH 3 were synthesized by the action of acids on Ph 5 Sb or on Ph 4 SbBr in the presence of Et 2 NH. According to X-ray diffraction analysis data, both compounds are antimony complexes with d...
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Published in: | Russian journal of general chemistry Vol. 91; no. 2; pp. 227 - 234 |
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01-02-2021
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Abstract | Tetraphenylantimony methacrylate Ph
4
SbO
2
CC(CH
3
)=CH
2
and tetraphenylantimony crotonate Ph
4
SbO
2
CCH=CHCH
3
were synthesized by the action of acids on Ph
5
Sb or on Ph
4
SbBr in the presence of Et
2
NH. According to X-ray diffraction analysis data, both compounds are antimony complexes with distorted tetragonal-pyramidal geometry. Polymerization of styrene with Ph
4
SbO
2
CC(CH
3
)=CH
2
and Ph
4
SbO
2
CCH=CHCH
3
additives gave transparent antimony-containing polystyrene soluble in chloroform, dichloromethane, and THF. |
---|---|
AbstractList | Tetraphenylantimony methacrylate Ph
4
SbO
2
CC(CH
3
)=CH
2
and tetraphenylantimony crotonate Ph
4
SbO
2
CCH=CHCH
3
were synthesized by the action of acids on Ph
5
Sb or on Ph
4
SbBr in the presence of Et
2
NH. According to X-ray diffraction analysis data, both compounds are antimony complexes with distorted tetragonal-pyramidal geometry. Polymerization of styrene with Ph
4
SbO
2
CC(CH
3
)=CH
2
and Ph
4
SbO
2
CCH=CHCH
3
additives gave transparent antimony-containing polystyrene soluble in chloroform, dichloromethane, and THF. Tetraphenylantimony methacrylate Ph.sub.4SbO.sub.2CC(CH.sub.3)=CH.sub.2 and tetraphenylantimony crotonate Ph.sub.4SbO.sub.2CCH=CHCH.sub.3 were synthesized by the action of acids on Ph.sub.5Sb or on Ph.sub.4SbBr in the presence of Et.sub.2NH. According to X-ray diffraction analysis data, both compounds are antimony complexes with distorted tetragonal-pyramidal geometry. Polymerization of styrene with Ph.sub.4SbO.sub.2CC(CH.sub.3)=CH.sub.2 and Ph.sub.4SbO.sub.2CCH=CHCH.sub.3 additives gave transparent antimony-containing polystyrene soluble in chloroform, dichloromethane, and THF. |
Audience | Academic |
Author | Ovsetsina, T. I. Gushchin, A. V. Maleeva, A. I. Somov, N. V. Tumanyan, A. S. Kipelkin, E. V. Andreev, P. V. |
Author_xml | – sequence: 1 givenname: A. V. surname: Gushchin fullname: Gushchin, A. V. email: gushchin4@yandex.ru organization: Lobachevsky State University of Nizhny Novgorod – sequence: 2 givenname: A. I. surname: Maleeva fullname: Maleeva, A. I. organization: Lobachevsky State University of Nizhny Novgorod – sequence: 3 givenname: E. V. surname: Kipelkin fullname: Kipelkin, E. V. organization: Lobachevsky State University of Nizhny Novgorod – sequence: 4 givenname: A. S. surname: Tumanyan fullname: Tumanyan, A. S. organization: Lobachevsky State University of Nizhny Novgorod – sequence: 5 givenname: P. V. surname: Andreev fullname: Andreev, P. V. organization: Lobachevsky State University of Nizhny Novgorod – sequence: 6 givenname: T. I. surname: Ovsetsina fullname: Ovsetsina, T. I. organization: Lobachevsky State University of Nizhny Novgorod – sequence: 7 givenname: N. V. surname: Somov fullname: Somov, N. V. organization: Lobachevsky State University of Nizhny Novgorod |
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CitedBy_id | crossref_primary_10_1016_j_mencom_2022_05_028 crossref_primary_10_31857_S0044460X23090093 crossref_primary_10_1134_S1070363223090098 crossref_primary_10_1134_S107032842208005X |
Cites_doi | 10.1134/S1063774518010170 10.3390/molecules19056009 10.1134/S0036023615060145 10.1016/j.jct.2018.11.011 10.1016/j.jfluchem.2020.109517 10.1134/S1070328414090073 10.1107/S002188980600731X 10.1107/S0021889899006020 10.1134/S0036024418090170 10.1107/S0108767307043930 10.1248/cpb.57.436 10.1021/cr9001269 10.31857/S0132344X20100011 10.1134/S107036321103008X 10.1023/A:1021165112211 10.1002/hc.20498 10.1134/S0036023620040178 10.1023/A:1011625728803 10.1039/c3dt51382c 10.1021/ma061220l 10.1039/DT9840001349 10.1080/10426508908046072 10.1134/S0036023615040221 10.1134/S003602361707021X 10.1021/ja01009a009 10.1016/j.jorganchem.2004.02.015 10.1134/S003602361402017X 10.1134/S0036023615030171 10.1134/S0036023619100139 10.1021/ma0622332 10.1039/DT9920001199 10.2174/092986707780362862 10.1023/A:102488332886 10.1134/S0036023614090174 10.1016/j.jorganchem.2009.07.041 10.1016/S0022-328X(00)82370-0 10.1002/hc.10208 10.1134/S0036023616020194 10.1039/CT9232302315 10.1023/B:RUCO.0000030159.74150.a1 10.1016/j.poly.2009.06.065 10.1016/S0022-328X(97)00759-6 10.1016/j.ica.2003.12.012 10.1007/s10973-017-6803-5 10.1016/j.jorganchem.2009.07.040 10.1002/aoc.491 10.1016/j.poly.2003.12.002 10.1134/S1070363209100107 10.1117/12.2086599 10.1016/j.jssc.2017.06.030 10.1134/S1070328418100020 |
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Keywords | antimony-containing polystyrene tetraphenylantimony methacrylate tetraphenylantimony crotonate |
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References | SharutinV.V.Poddel’skyA.I.SharutinaO.K.Russ. J. Coord. Chem.2020466631:CAS:528:DC%2BB3cXhvFCgsL%2FL10.31857/S0132344X20100011 SharutinV.V.SenchurinV.S.SharutinaO.K.PakusinaA.P.SmirnovaS.A.Russ. J. Gen. Chem.20097921311:CAS:528:DC%2BD1MXhsFCgsLnN10.1134/S1070363209100107 SharutinV.V.SharutinaO.K.EfremovA.N.Artem’evaE.V.Russ. J. Inorg. Chem.20196412291:CAS:528:DC%2BC1MXitFanurbK10.1134/S0036023619100139 ShenK.W.McEwenW.E.LaPlacaL.J.HamiltonW.C.WolfA.P.J. Am. Chem. Soc.19689017181:CAS:528:DyaF1cXpvFGgug%3D%3D10.1021/ja01009a009 GibbonsN.SowerbyD.B.J. Organomet. Chem.19985552711:CAS:528:DyaK1cXhvFCrurw%3D10.1016/S0022-328X(97)00759-6 LeebrickJ.R.RemesN.L.Chem. Abstr.19717498851 SomovN.V.AndreevP.V.Crystallogr. Rep.201863321:CAS:528:DC%2BC1cXjvVShsbc%3D10.1134/S1063774518010170 AddisonA.W.RaoT.N.ReedijkJ.van RijnJ.VerschoorG.C.J. Chem. Soc. Dalton Trans.19847134910.1039/DT9840001349 MacraeC.F.EdgingtonP.R.McCabeP.PidcockE.ShieldsG.P.TaylorR.TowlerM.van de StreekJ.J. Appl. Cryst.2006394531:CAS:528:DC%2BD28Xkslehsbk%3D10.1107/S002188980600731X GushchinA.V.ShashkinD.V.PrytkovaL.K.SomovN.V.BaranovE.V.ShavyrinA.S.RykalinV.I.Russ. J. Gen. Chem.2011814931:CAS:528:DC%2BC3MXkvVyjtrw%3D10.1134/S107036321103008X QuanL.YinH.CuiJ.-C.CuiL.HongM.WangD.YangM.J. Organomet. Chem.200969436831:CAS:528:DC%2BD1MXht1amtL3I10.1016/j.jorganchem.2009.07.041 YuL.MaY.-Q.WangG.-C.LiJ.-S.Heteroatom Chem.200415321:CAS:528:DC%2BD2cXmsFWkug%3D%3D10.1002/hc.10208 IslamA.Da SilvaJ.G.BerbetF.M.Da SilvaS.M.RodriguesB.L.BeraldoH.MeloM.N.FrezardF.DemicheliC.Molecules20141960091:CAS:528:DC%2BC2cXht1GjtLvP10.3390/molecules19056009248241366271143 YinH.-D.WenL.-Y.CuiJ.-C.LiW.-K.Polyhedron20092829191:CAS:528:DC%2BD1MXhtV2ktLzO10.1016/j.poly.2009.06.065 CrysAlis CCD and CrysAlis RED, Rigaku Oxford Diffraction, 2015 GushchinA.V.ShashkinD.V.ShcherbakovaT.S.SomovN.V.FukinG.K.ShavyrinA.S.RykalinV.I.DodonovV.A.Vestn. Nizhegor. Univ., Ser. Khim.2010668 SharutinV.V.PakusinaA.P.PlatonovaT.P.EgorovaI.V.SharutinaO.K.GerasimenkoA.V.SergienkoA.S.GerasimenkoE.A.Russ. J. Coord. Chem.2002287531:CAS:528:DC%2BD38XoslOjsL4%3D10.1023/A:1021165112211 MishraJ.SaxenaA.SinghS.Curr. Med. Chem.20071411531:CAS:528:DC%2BD2sXksVKqsrw%3D10.2174/09298670778036286217456028 LeebrickJ.R.Chem. Abstr.19676685070 Carraher, Ch.E., Jr., and Moran, M., in Organometallic Polymers, Carraher, Ch.E., Jr., Sheats, J.E., and Pittman, C.U.Jr., Eds.., New York: Academic, 1978. YuL.MaY.-Q.LiuR.-C.WangG.-C.LiJ.-S.DuG.-H.HuJ.-J.Polyhedron2004238231:CAS:528:DC%2BD2cXht12rt7s%3D10.1016/j.poly.2003.12.002 Gushchin, A.V., Kalistratova, O.S., Verkhovykh, R.A., Somov, N.V., Shashkin, D.V., and Dodonov, V.A., Vestn. Nizhegor. Univ., Ser. Khim., 2013, issue 1(1), p. 86. DoakG.O.LongG.G.FreedmanL.D.J. Organomet. Chem.19654821:CAS:528:DyaF2MXktFCnsrs%3D10.1016/S0022-328X(00)82370-0 SharutinV.V.SharutinaO.K.Russ. J. Inorg. Chem.2015602921:CAS:528:DC%2BC2MXltFChsro%3D10.1134/S0036023615030171 QuanL.YinH.CuiJ-C.HongM.WangD.J. Organomet. Chem.200969437081:CAS:528:DC%2BD1MXht1amtL3E10.1016/j.jorganchem.2009.07.040 FukinG.K.SamsonovM.A.BaranovE.V.CherkasovA.V.RumyantsevR.V.ArapovaA.V.Russ. J. Coord. Chem.2018446261:CAS:528:DC%2BC1cXhvVKmsrfI10.1134/S1070328418100020 SharutinV.V.SharutinaO.K.Russ. J. Coord. Chem.2014406431:CAS:528:DC%2BC2cXhsVKmtrrM10.1134/S1070328414090073 GoddardA.E.J. Chem. Soc.192312323151:CAS:528:DyaB2cXktVw%3D10.1039/CT9232302315 SharutinV.V.SharutinaO.K.SenchurinS.V.Russ. J. Inorg. Chem.2014599511:CAS:528:DC%2BC2cXhsVKmtrnF10.1134/S0036023614090174 LiuR.-C.MaY.-Q.YuL.LiJ.-S.CuiJ.-R.WangR.-Q.Appl. Organomet. Chem.2003176621:CAS:528:DC%2BD3sXmvFOrt7c%3D10.1002/aoc.491 DodonovV.A.GushchinA.V.KuznetsovaYu.L.MorugovaV.A.Vestn. Nizhegor. Univ., Ser. Khim.2004186 Farrugia, L.J., J. Appl. Cryst., 1999, vol. 32, p. 837. https://doi.org/10.1107/S0021889899006020 FukinG.K.SamsonovM.A.ArapovaA.V.MazurA.S.ArtamonovaT.O.KhodorkovskiyM.A.VasilyevA.V.J. Solid State Chem.2017254321:CAS:528:DC%2BC2sXhtFCqsrvF10.1016/j.jssc.2017.06.030 NakaK.NakahashiA.ChujoY.Macromolecules20074013721:CAS:528:DC%2BD2sXhtlymsrc%3D10.1021/ma0622332 SharutinV.V.SenchurinV.S.SharutinaO.K.Russ. J. Inorg. Chem.2014591151:CAS:528:DC%2BC2cXivFyjsLg%3D10.1134/S003602361402017X SharutinV.V.SharutinaO.K.KhnykinaK.A.Russ. J. Inorg. Chem.2016611801:CAS:528:DC%2BC28XlsVOkt7c%3D10.1134/S0036023616020194 Millington, P.L. and Sowerby, D.B., J. Chem. Soc. Dalton Trans., 1992, p. 1199. https://doi.org/10.1039/DT9920001199 LeebrickJ.R.RemesN.L.Chem. Abstr.196868105367 LyakaevD.V.MarkinA.V.KhabarovaE.V.SmirnovaN.N.KnyazevA.V.SharutinV.V.SharutinaO.K.Russ. J. Phys. Chem. A20189216591:CAS:528:DC%2BC1cXhs1Kgu7fO10.1134/S0036024418090170 LyakaevD.V.MarkinA.V.SmirnovaN.N.SharutinV.V.SharutinaO.K.J. Therm. Anal. Calorim.201713311431:CAS:528:DC%2BC2sXhslyrtLfE10.1007/s10973-017-6803-5 LiJ.-S.LiuR.-C.ChiX.-B.WangG.-C.GuoQ.-S.Inorg. Chim. Acta200435721761:CAS:528:DC%2BD2cXislyit7s%3D10.1016/j.ica.2003.12.012 SharutinV.V.SharutinaO.K.SenchurinV.S.Russ. J. Inorg. Chem.20156010931:CAS:528:DC%2BC2MXhsVagtrbK10.1134/S0036023615060145 SharutinV.V.SharutinaO.K.KotlyarovA.R.Russ. J. Inorg. Chem.2015604651:CAS:528:DC%2BC2MXmsFersro%3D10.1134/S0036023615040221 Kocheshkov, K.A., Skoldinov, A.P., and Zemlyanskii, N.N., Metody elementoorganicheskoi khimii. Sur’ma, vismut (Methods of Organoelement Chemistry: Antimony, Bismuth), Moscow: Nauka, 1976. WangG.C.XiaoJ.YuL.LiJ.-S.CuiJ.-R.WangR.-Q.RanF.X.J. Organomet. Chem.200468916311:CAS:528:DC%2BD2cXjtVentb0%3D10.1016/j.jorganchem.2004.02.015 SheldrickG.M.Acta Crystallogr., Sect. A2008641121:CAS:528:DC%2BD2sXhsVGhurzO10.1107/S010876730704393018156677 Koton, M.M., Metalloorganicheskie soedineniya i radikaly (Organometallic Compounds and Radicals), Moscow: Nauka, 1985, p.13. NakaK.NakahashiA.ChujoY.Macromolecules20063982571:CAS:528:DC%2BD28Xht1Wmtr3O10.1021/ma061220l SharutinV.V.SharutinaO.K.Russ. J. Inorg. Chem.2017629051:CAS:528:DC%2BC2sXht1ygurvE10.1134/S003602361707021X Batsanov, S.S., Inorg. Mater., 2001, vol. 37, no. 9, p. 871. https://doi.org/10.1023/A:1011625728803 LyakaevD.V.MarkinA.V.SmirnovaN.N.SharutinV.V.SharutinaO.K.J. Chem. Thermodyn.20191313221:CAS:528:DC%2BC1cXitlaksb%2FK10.1016/j.jct.2018.11.011 SharutinV.V.PakusinaA.P.ZadachinaO.P.SharutinaO.K.GerasimenkoA.V.PushilinM.A.Russ. J. Coord. Chem.2004303971:CAS:528:DC%2BD2cXksFGlu7w%3D10.1023/B:RUCO.0000030159.74150.a1 QinW.KakusawaN.WuY.YasuikeS.KuritaJ.Chem. Pharm. Bull.2009574361:CAS:528:DC%2BD1MXmtl2msLY%3D10.1248/cpb.57.436 BoneS.P.SowerbyD.B.hosphorus, Sulfur, Silicon, Relat. Elem.1989452321:CAS:528:DyaK3cXhsl2htrc%3D10.1080/10426508908046072 PassarelliJ.MurphyM.Del ReR.SortlandM.DousharmL.VockenhuberM.EkinciY.NeisserM.FreedmanD.A.BrainardR.L.Adv. Pattern. Mater. Proc. XXXII201594259425010.1117/12.2086599 SharutinV.V.SharutinaO.K.Bondar’E.V.PakusinaA.P.AdoninN.Yu.StarichenkoV.F.Russ. J. Gen. Chem.2002723901:CAS:528:DC%2BB3cXosVSrtb0%3D10.1016/j.jfluchem.2020.109517 SharutinV.V.SharutinaO.K.EfremovA.N.Artem’evaE.V.Russ. J. Inorg. Chem.2020655021:CAS:528:DC%2BB3cXot1ClsL4%3D10.1134/S0036023620040178 GushchinA.V.GrunovaE.V.MoiseevD.V.MorozovO.S.ShavyrinA.S.DodonovV.A.Russ. Chem. Bull.20035213761:CAS:528:DC%2BD3sXlslSiu7Y%3D10.1023/A:102488332886 IslamA.DaSilvaJ.G.BerbetF.M.DaSilvaS.M.RodriguesB.L.BeraldoH.MeloM.N.Molecules20141960091:CAS:528:DC%2BC2cXht1GjtLvP10.3390/molecules19056009248241366271143 AliM.I.RaufM.K.BadshahA.KumarI.ForsythC.M.JunkP.C.KedzierskiL.AndrewsP.C.Dalton Trans.201342167331:CAS:528:DC%2BC3sXhvVSnu77M10.1039/c3dt51382c24077559 YamagoS.Chem. Rev.200910950511:CAS:528:DC%2BD1MXhtVGktbrE10.1021/cr900126919711982 SinghalK.MishraR.RajP.Heteroatom Chem.2008196881:CAS:528:DC%2BD1cXhsVKgt73J10.1002/hc.20498 A. Islam (5379_CR2) 2014; 19 A.E. Goddard (5379_CR6) 1923; 123 A.V. Gushchin (5379_CR25) 2010; 6 V.V. Sharutin (5379_CR29) 2020; 65 A.W. Addison (5379_CR58) 1984; 7 A.V. Gushchin (5379_CR62) 2011; 81 V.V. Sharutin (5379_CR39) 2014; 59 5379_CR47 S.P. Bone (5379_CR26) 1989; 45 J. Passarelli (5379_CR20) 2015; 9425 V.V. Sharutin (5379_CR32) 2014; 59 J.R. Leebrick (5379_CR22) 1968; 68 G.M. Sheldrick (5379_CR53) 2008; 64 V.V. Sharutin (5379_CR28) 2015; 60 V.V. Sharutin (5379_CR35) 2017; 62 J. Mishra (5379_CR1) 2007; 14 S. Yamago (5379_CR19) 2009; 109 V.V. Sharutin (5379_CR40) 2009; 79 J.-S. Li (5379_CR52) 2004; 357 G.K. Fukin (5379_CR63) 2018; 44 G.K. Fukin (5379_CR61) 2017; 254 L. Quan (5379_CR51) 2009; 694 D.V. Lyakaev (5379_CR42) 2017; 133 L. Yu (5379_CR10) 2004; 23 L. Yu (5379_CR11) 2004; 15 5379_CR18 G.C. Wang (5379_CR9) 2004; 689 5379_CR59 V.V. Sharutin (5379_CR43) 2002; 28 L. Quan (5379_CR50) 2009; 694 5379_CR54 5379_CR55 V.A. Dodonov (5379_CR24) 2004; 1 V.V. Sharutin (5379_CR37) 2015; 60 J.R. Leebrick (5379_CR21) 1971; 74 J.R. Leebrick (5379_CR12) 1967; 66 W. Qin (5379_CR45) 2009; 57 N.V. Somov (5379_CR57) 2018; 63 K. Singhal (5379_CR13) 2008; 19 A.V. Gushchin (5379_CR46) 2003; 52 D.V. Lyakaev (5379_CR38) 2019; 131 V.V. Sharutin (5379_CR44) 2002; 72 V.V. Sharutin (5379_CR30) 2020; 46 V.V. Sharutin (5379_CR34) 2015; 60 G.O. Doak (5379_CR7) 1965; 4 5379_CR64 5379_CR23 5379_CR60 V.V. Sharutin (5379_CR33) 2014; 40 V.V. Sharutin (5379_CR36) 2019; 64 M.I. Ali (5379_CR3) 2013; 42 N. Gibbons (5379_CR4) 1998; 555 K. Naka (5379_CR17) 2006; 39 K.W. Shen (5379_CR5) 1968; 90 R.-C. Liu (5379_CR8) 2003; 17 A. Islam (5379_CR15) 2014; 19 V.V. Sharutin (5379_CR27) 2004; 30 V.V. Sharutin (5379_CR31) 2016; 61 D.V. Lyakaev (5379_CR41) 2018; 92 H.-D. Yin (5379_CR49) 2009; 28 J. Mishra (5379_CR14) 2007; 14 K. Singhal (5379_CR48) 2008; 19 C.F. Macrae (5379_CR56) 2006; 39 K. Naka (5379_CR16) 2007; 40 |
References_xml | – volume: 66 start-page: 85070 year: 1967 ident: 5379_CR12 publication-title: Chem. Abstr. contributor: fullname: J.R. Leebrick – ident: 5379_CR60 – volume: 63 start-page: 32 year: 2018 ident: 5379_CR57 publication-title: Crystallogr. Rep. doi: 10.1134/S1063774518010170 contributor: fullname: N.V. Somov – ident: 5379_CR64 – volume: 19 start-page: 6009 year: 2014 ident: 5379_CR15 publication-title: Molecules doi: 10.3390/molecules19056009 contributor: fullname: A. Islam – volume: 60 start-page: 1093 year: 2015 ident: 5379_CR37 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023615060145 contributor: fullname: V.V. Sharutin – volume: 131 start-page: 322 year: 2019 ident: 5379_CR38 publication-title: J. Chem. Thermodyn. doi: 10.1016/j.jct.2018.11.011 contributor: fullname: D.V. Lyakaev – volume: 72 start-page: 390 year: 2002 ident: 5379_CR44 publication-title: Russ. J. Gen. Chem. doi: 10.1016/j.jfluchem.2020.109517 contributor: fullname: V.V. Sharutin – volume: 40 start-page: 643 year: 2014 ident: 5379_CR33 publication-title: Russ. J. Coord. Chem. doi: 10.1134/S1070328414090073 contributor: fullname: V.V. Sharutin – volume: 68 start-page: 105367 year: 1968 ident: 5379_CR22 publication-title: Chem. Abstr. contributor: fullname: J.R. Leebrick – volume: 39 start-page: 453 year: 2006 ident: 5379_CR56 publication-title: J. Appl. Cryst. doi: 10.1107/S002188980600731X contributor: fullname: C.F. Macrae – ident: 5379_CR54 doi: 10.1107/S0021889899006020 – volume: 92 start-page: 1659 year: 2018 ident: 5379_CR41 publication-title: Russ. J. Phys. Chem. A doi: 10.1134/S0036024418090170 contributor: fullname: D.V. Lyakaev – volume: 64 start-page: 112 year: 2008 ident: 5379_CR53 publication-title: Acta Crystallogr., Sect. A doi: 10.1107/S0108767307043930 contributor: fullname: G.M. Sheldrick – ident: 5379_CR55 – volume: 57 start-page: 436 year: 2009 ident: 5379_CR45 publication-title: Chem. Pharm. Bull. doi: 10.1248/cpb.57.436 contributor: fullname: W. Qin – volume: 109 start-page: 5051 year: 2009 ident: 5379_CR19 publication-title: Chem. Rev. doi: 10.1021/cr9001269 contributor: fullname: S. Yamago – volume: 46 start-page: 663 year: 2020 ident: 5379_CR30 publication-title: Russ. J. Coord. Chem. doi: 10.31857/S0132344X20100011 contributor: fullname: V.V. Sharutin – volume: 81 start-page: 493 year: 2011 ident: 5379_CR62 publication-title: Russ. J. Gen. Chem. doi: 10.1134/S107036321103008X contributor: fullname: A.V. Gushchin – volume: 28 start-page: 753 year: 2002 ident: 5379_CR43 publication-title: Russ. J. Coord. Chem. doi: 10.1023/A:1021165112211 contributor: fullname: V.V. Sharutin – ident: 5379_CR23 – volume: 19 start-page: 688 year: 2008 ident: 5379_CR13 publication-title: Heteroatom Chem. doi: 10.1002/hc.20498 contributor: fullname: K. Singhal – volume: 65 start-page: 502 year: 2020 ident: 5379_CR29 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023620040178 contributor: fullname: V.V. Sharutin – ident: 5379_CR59 doi: 10.1023/A:1011625728803 – volume: 42 start-page: 16733 year: 2013 ident: 5379_CR3 publication-title: Dalton Trans. doi: 10.1039/c3dt51382c contributor: fullname: M.I. Ali – volume: 39 start-page: 8257 year: 2006 ident: 5379_CR17 publication-title: Macromolecules doi: 10.1021/ma061220l contributor: fullname: K. Naka – volume: 7 start-page: 1349 year: 1984 ident: 5379_CR58 publication-title: J. Chem. Soc. Dalton Trans. doi: 10.1039/DT9840001349 contributor: fullname: A.W. Addison – volume: 45 start-page: 23 year: 1989 ident: 5379_CR26 publication-title: hosphorus, Sulfur, Silicon, Relat. Elem. doi: 10.1080/10426508908046072 contributor: fullname: S.P. Bone – volume: 19 start-page: 688 year: 2008 ident: 5379_CR48 publication-title: Heteroatom Chem. doi: 10.1002/hc.20498 contributor: fullname: K. Singhal – volume: 60 start-page: 465 year: 2015 ident: 5379_CR28 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023615040221 contributor: fullname: V.V. Sharutin – volume: 62 start-page: 905 year: 2017 ident: 5379_CR35 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S003602361707021X contributor: fullname: V.V. Sharutin – volume: 90 start-page: 1718 year: 1968 ident: 5379_CR5 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja01009a009 contributor: fullname: K.W. Shen – volume: 689 start-page: 1631 year: 2004 ident: 5379_CR9 publication-title: J. Organomet. Chem. doi: 10.1016/j.jorganchem.2004.02.015 contributor: fullname: G.C. Wang – volume: 74 start-page: 98851 year: 1971 ident: 5379_CR21 publication-title: Chem. Abstr. contributor: fullname: J.R. Leebrick – volume: 6 start-page: 68 year: 2010 ident: 5379_CR25 publication-title: Vestn. Nizhegor. Univ., Ser. Khim. contributor: fullname: A.V. Gushchin – volume: 59 start-page: 115 year: 2014 ident: 5379_CR32 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S003602361402017X contributor: fullname: V.V. Sharutin – ident: 5379_CR18 – volume: 60 start-page: 292 year: 2015 ident: 5379_CR34 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023615030171 contributor: fullname: V.V. Sharutin – volume: 19 start-page: 6009 year: 2014 ident: 5379_CR2 publication-title: Molecules doi: 10.3390/molecules19056009 contributor: fullname: A. Islam – volume: 64 start-page: 1229 year: 2019 ident: 5379_CR36 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023619100139 contributor: fullname: V.V. Sharutin – volume: 40 start-page: 1372 year: 2007 ident: 5379_CR16 publication-title: Macromolecules doi: 10.1021/ma0622332 contributor: fullname: K. Naka – ident: 5379_CR47 doi: 10.1039/DT9920001199 – volume: 14 start-page: 1153 year: 2007 ident: 5379_CR1 publication-title: Curr. Med. Chem. doi: 10.2174/092986707780362862 contributor: fullname: J. Mishra – volume: 52 start-page: 1376 year: 2003 ident: 5379_CR46 publication-title: Russ. Chem. Bull. doi: 10.1023/A:102488332886 contributor: fullname: A.V. Gushchin – volume: 59 start-page: 951 year: 2014 ident: 5379_CR39 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023614090174 contributor: fullname: V.V. Sharutin – volume: 694 start-page: 3683 year: 2009 ident: 5379_CR51 publication-title: J. Organomet. Chem. doi: 10.1016/j.jorganchem.2009.07.041 contributor: fullname: L. Quan – volume: 4 start-page: 82 year: 1965 ident: 5379_CR7 publication-title: J. Organomet. Chem. doi: 10.1016/S0022-328X(00)82370-0 contributor: fullname: G.O. Doak – volume: 15 start-page: 32 year: 2004 ident: 5379_CR11 publication-title: Heteroatom Chem. doi: 10.1002/hc.10208 contributor: fullname: L. Yu – volume: 61 start-page: 180 year: 2016 ident: 5379_CR31 publication-title: Russ. J. Inorg. Chem. doi: 10.1134/S0036023616020194 contributor: fullname: V.V. Sharutin – volume: 123 start-page: 2315 year: 1923 ident: 5379_CR6 publication-title: J. Chem. Soc. doi: 10.1039/CT9232302315 contributor: fullname: A.E. Goddard – volume: 14 start-page: 1153 year: 2007 ident: 5379_CR14 publication-title: Curr. Med. Chem. doi: 10.2174/092986707780362862 contributor: fullname: J. Mishra – volume: 1 start-page: 86 year: 2004 ident: 5379_CR24 publication-title: Vestn. Nizhegor. Univ., Ser. Khim. contributor: fullname: V.A. Dodonov – volume: 30 start-page: 397 year: 2004 ident: 5379_CR27 publication-title: Russ. J. Coord. Chem. doi: 10.1023/B:RUCO.0000030159.74150.a1 contributor: fullname: V.V. Sharutin – volume: 28 start-page: 2919 year: 2009 ident: 5379_CR49 publication-title: Polyhedron doi: 10.1016/j.poly.2009.06.065 contributor: fullname: H.-D. Yin – volume: 555 start-page: 271 year: 1998 ident: 5379_CR4 publication-title: J. Organomet. Chem. doi: 10.1016/S0022-328X(97)00759-6 contributor: fullname: N. Gibbons – volume: 357 start-page: 2176 year: 2004 ident: 5379_CR52 publication-title: Inorg. Chim. Acta doi: 10.1016/j.ica.2003.12.012 contributor: fullname: J.-S. Li – volume: 133 start-page: 1143 year: 2017 ident: 5379_CR42 publication-title: J. Therm. Anal. Calorim. doi: 10.1007/s10973-017-6803-5 contributor: fullname: D.V. Lyakaev – volume: 694 start-page: 3708 year: 2009 ident: 5379_CR50 publication-title: J. Organomet. Chem. doi: 10.1016/j.jorganchem.2009.07.040 contributor: fullname: L. Quan – volume: 17 start-page: 662 year: 2003 ident: 5379_CR8 publication-title: Appl. Organomet. Chem. doi: 10.1002/aoc.491 contributor: fullname: R.-C. Liu – volume: 23 start-page: 823 year: 2004 ident: 5379_CR10 publication-title: Polyhedron doi: 10.1016/j.poly.2003.12.002 contributor: fullname: L. Yu – volume: 79 start-page: 2131 year: 2009 ident: 5379_CR40 publication-title: Russ. J. Gen. Chem. doi: 10.1134/S1070363209100107 contributor: fullname: V.V. Sharutin – volume: 9425 start-page: 94250 year: 2015 ident: 5379_CR20 publication-title: Adv. Pattern. Mater. Proc. XXXII doi: 10.1117/12.2086599 contributor: fullname: J. Passarelli – volume: 254 start-page: 32 year: 2017 ident: 5379_CR61 publication-title: J. Solid State Chem. doi: 10.1016/j.jssc.2017.06.030 contributor: fullname: G.K. Fukin – volume: 44 start-page: 626 year: 2018 ident: 5379_CR63 publication-title: Russ. J. Coord. Chem. doi: 10.1134/S1070328418100020 contributor: fullname: G.K. Fukin |
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Snippet | Tetraphenylantimony methacrylate Ph
4
SbO
2
CC(CH
3
)=CH
2
and tetraphenylantimony crotonate Ph
4
SbO
2
CCH=CHCH
3
were synthesized by the action of acids on... Tetraphenylantimony methacrylate Ph.sub.4SbO.sub.2CC(CH.sub.3)=CH.sub.2 and tetraphenylantimony crotonate Ph.sub.4SbO.sub.2CCH=CHCH.sub.3 were synthesized by... |
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StartPage | 227 |
SubjectTerms | Acrylates Chemistry Chemistry and Materials Science Chemistry/Food Science Polymerization Polystyrene |
Title | Synthesis and Structure of Tetraphenylantimony Methacrylate and Tetraphenylantimony Crotonate and Their Use for the Production of Antimony-Containing Polystyrene |
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