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Synthesis of star polymers of styrene and alkyl (meth)acrylates from a porphyrin initiator core via ATRP

机译:卟啉引发剂核通过ATRP合成苯乙烯和(甲基)丙烯酸烷基酯的星形聚合物

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摘要

A free-base tetrabromoporphyrin, 15,20-tetrakis(4-(2-methyl-2-bromopropoxy)phenyl)-21H,23H-porphine (2), was synthesized in high yield (91%) by the esterification of 5,10,15,20-tetrakis(4-hydroxyphenyl)-21H, 23H-porphine (1) with 2-bromo-2-methylpropanoyl bromide. The free-base porphyrin (2) was demonstrated to be suitable as an initiator for atom transfer radical polymerization (ATRP) of methyl methacrylate giving porphyrin-core star-poly(methyl methacrylate) with conversions of up to 98% ((CuBr)-Br-I, N-(n-propyl)-2-pyridyl-methanimine, toluene, 90 degrees C). UV-vis spectroscopic analysis demonstrated that a degree of complexation of Cu(II) by the porphyrin core occurred during the polymerization. To avoid Cu(11) complexation, zinc(II) 10,15,20-tetrakis(4-(2-methyl-2-bromopropoxy)phenyl)-21H,23H-porphine (4) was synthesized from the free-base porphyrin (2) and employed as an initiator in the ATRP of MMA, giving the corresponding Zn porphyrin-core star-PMMA. The free-base porphyrin (2) was also employed as an initiator for the polymerization of styrene, methyl acrylate, butyl methacrylate, octadecyl acrylate and the copolymerization of isobutyl methacrylate (IBMA) and trifluoroethyl methacrylate (TFEMA), in all cases giving star polymers with conversions of 33-87%. Basic hydrolysis of a porphyrin-core star-polystyrene polymer cleaved the ester linkages about the porphyrin, liberating the individual polystyrene chains which had a number-average molecular weight approximately one-fourth that of the precursor star polymer and a narrow polydispersity index (M-w/M-n, = 1.15) thereby demonstrating efficient initiation from the porphyrin core. Palladium(II) 10,15,20-tetrakis(4-(2-methyl-2-bromopropoxy)phenyl)-21H,23H-porphine (3) was synthesized from the free-base porphyrin (2) and employed as an initiator in the ATRP of MMA but the polymerization was completely inhibited. Pd(II) was introduced into the star polymer cores by heating either a solution of the porphyrin-core star-PMMA or the Zn porphyrin-core star-PMMA with (PdCl2)-Cl-II in benzonitrile. Pt(II) was introduced into a star polymer core by heating a solution of the Zn porphyrin-core star-PMMA-co-TFEMA with (PtCl2)-Cl-II in benzonitrile. UV-vis spectroscopic analysis confirmed the synthesis of Pd(11) and Pt(II) porphyrin complexes and photoluminescent spectroscopy confirmed the luminescent properties of the materials.
机译:通过5的酯化反应以高收率(91%)合成了游离碱四溴卟啉15,20-四(4-(2-甲基-2-溴丙氧基)苯基)-21H,23H-卟啉(2)。 10,15,20-四(4-羟苯基)-21H,23H-卟啉(1)与2-溴-2-甲基丙酰溴。游离碱卟啉(2)已证明适合用作甲基丙烯酸甲酯的原子转移自由基聚合(ATRP)的引发剂,从而得到卟啉芯的星形聚甲基丙烯酸甲酯,转化率高达98% Br-I,N-(正丙基)-2-吡啶基-甲亚胺,甲苯,90℃。紫外-可见光谱分析表明,在聚合过程中,卟啉核发生了一定程度的Cu(II)络合。为避免Cu(11)络合,从游离碱卟啉合成了锌(II)10,15,20-四(4-(2-甲基-2-溴丙氧基)苯基)-21H,23H-吗啡(4) (2)并用作MMA ATRP的引发剂,得到相应的锌卟啉核星形PMMA。游离碱卟啉(2)还用作引发剂,用于苯乙烯,丙烯酸甲酯,甲基丙烯酸丁酯,丙烯酸十八烷基酯的聚合以及甲基丙烯酸异丁酯(IBMA)和甲基丙烯酸三氟乙酯(TFEMA)的共聚,在所有情况下均得到星形聚合物转换率为33-87%。卟啉核心的星形聚苯乙烯聚合物的碱性水解裂解了卟啉周围的酯键,释放出单聚苯乙烯链,其数均分子量约为前星形聚合物的四分之一,并且多分散指数(Mw / Mn = 1.15)由此证明了从卟啉核心的有效引发。由游离碱卟啉(2)合成钯(II)10,15,20-四(4-(2-甲基-2-溴丙氧基)苯基)-21H,23H-卟啉(3)在MMA的ATRP中,但是聚合被完全抑制。通过加热卟啉核心星形PMMA或Zn卟啉核心星形PMMA与(PdCl2)-Cl-II在苄腈中的溶液将Pd(II)引入星形聚合物核心。通过加热锌卟啉核星形-PMMA-co-TFEMA与(PtCl2)-Cl-II在苄腈中的溶液,将Pt(II)引入星形聚合物核。紫外可见光谱分析证实了Pd(11)和Pt(II)卟啉配合物的合成,光致发光光谱证实了材料的发光特性。

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