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SYNTHESIS AND POLYMERIZATION OF SUBSTITUTED ARYL VINYL SULFOXIDES - ON-LINE MONITORING AND KINETICS OF THE THERMAL DEGRADATION OF POLYMERIC SULFOXIDES INTO TRANS-POLYACETYLENE

机译:取代的芳基乙烯基硫化物的合成和聚合-聚合物硫化物热转化为反型聚乙烯的在线监测和动力学

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The substituted aryl vinyl sulfoxides p-[RC(6)H(4)S(O)CH=CH2] (8a-c, R = F, Cl, OMe) were prepared and polymerized in the presence of(3-methyl-1,1-diphenylpentyl)lithium (MDPPLi, 1) as anionic initiator to give the corresponding poly(aryl vinyl sulfoxides) 9a-c. Upon thermolysis of compounds 9 between 70 and 120 degrees C, the arenesulfenic acids (10) were eliminated via an Ei mechanism generating all-trans-polyacetylene (PA, 11). The formation of all-trans-PA was monitored on-line by means of near-infrared-excited Fourier-transform (FT)-Raman spectroscopy. The kinetics of the reaction were found to be first-order at conversions above approximately 10%. On the basis of the rate constants determined for the thermolysis of 9a-c at 70, 80, 90, 100, and 120 degrees C, the relative reactivities of 9a-c, and thus the influence of the substituents R on the rate of the PA formation, could be quantitatively estimated, and the following ratios were found: 9a (R = F):9b (R = Cl):9c (R = OMe) = 1.0 +/- 0.1:2.2 +/- 0.3:0.8 +/- 0.1. [References: 57]
机译:制备了取代的芳基乙烯基亚砜p- [RC(6)H(4)S(O)CH = CH2](8a-c,R = F,Cl,OMe),并在(3-甲基- 1,1-二苯基戊基)锂(MDPPLi,1)作为阴离子引发剂,得到相应的聚(芳基乙烯基亚砜)9a-c。在70到120摄氏度之间热解化合物9时,通过Ei机理消除了芳烃亚磺酸(10),生成了全反式聚乙炔(PA,11)。通过近红外激发傅里叶变换(FT)-拉曼光谱在线监测全反式PA的形成。发现反应的动力学是一级的,转化率高于约10%。根据在70、80、90、100和120摄氏度下热解9a-c所确定的速率常数,可以确定9a-c的相对反应性,以及因此取代基R对其反应速率的影响。可以定量估计PA的形成情况,发现以下比率:9a(R = F):9b(R = Cl):9c(R = OMe)= 1.0 +/- 0.1:2.2 +/- 0.3:0.8 + /-0.1。 [参考:57]

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