聚异丁烯高活性端基含量及相对分子质量测定方法的研究

综合使用核磁，VPO和近红外光谱分析技术对聚异丁烯活性端基含量以及相对分子质量的测定进行了详细研究，分别建立核测定聚异丁烯活性端基含量以及其他烯键含量和近红外光谱快速测量聚异聚丁烯活性端基含量。其他烯键含量和相对分子质量的分析方法。成对t检验结果表明，近红外光谱分析方法测定结果与核磁和VPO方法测定结果之间无显著性差异。     

Synthesis and catalytic application of monometallic molybdenum(IV) nitrile complexes

The novel molybdenum(IV) compound [MoO(NCMe)₅][B(C₆F₅)₄]₂ (1a) has been prepared by air oxidation of [Mo(CO)₃(NCMe)₃] in the presence of [H(OEt₂)₂][B(C₆F₅)₄] at room temperature. The [MoO(NCMe)₅]²⁺ cation shows a distorted octahedral configuration with two different acetonitrile-metal bond lengths due to a trans effect of the oxo-ligand. The trans-acetonitrile ligand is easily abstracted under oil pump vacuum to form [MoO(NCMe)₄][B(C₆F₅)₄]₂ (1b). The complex [MoO(NCPh)₄][B(C₆F₅)₄]₂ (2) is formed by substitution of acetonitrile ligands of 1a with benzonitrile molecules. The Mo(IV) complexes can be applied in the homopolymerization of isobutene at 30 °C leading to high yields and moderate molecular weights.     

Synthesis of Poly(IB‐co‐VBDC)‐g‐PMMA via Photo‐initiated Free Radical Graft Polymerization

Abstract

Photoinitiated free radical graft polymerization of methyl methacrylate (MMA) with poly[isobutene‐co‐(4‐vinyl benzyl N,N‐diethyldithiocarbamate)] [poly(IB‐co‐VBDC)] as macromolecular iniferter was investigated. The polymerization proceeds to give a high yield graft copolymer, however it was observed that even in the early stage of the polymerization there formed an insoluble polymer. In the presence of tetraethylthiuram disulfide (TETD) the gel fraction of the yield graft copolymer was drastically reduced and the polymerization was retarded as well. When the [TETD]/[VBDC] increased from 0 to 1.0, the gel fraction of the graft copolymer decreased from 33.2% to 1.6% (wt) while the fraction of the homopolymer of the MMA increased from 4.5% to 10.5% (wt). With the increasing of the UV irradiation time, both the MMA conversion and the molecular weight of the graft copolymer increased readily.