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Bulk Polymerization of (L,L)-Lactide Using Non-Organometallic Triazolium Carbene: Limited Advantages

机译:使用非有机金属三唑碳烯进行(L,L)-丙交酯的本体聚合:有限的优势

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The ring-opening polymerization (ROP) of L,L-lactide (L-LA) has been studied in bulk using alcohol (eithermethanol or benzyl alcohol) and 1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene carbene, 1, respectively as initiatorand non-organometallic catalyst, over a range of temperature and alcohol-to-1 molar ratios. Although 1 is known toperfectly control the polymerization of L-LA in solution at 90°C, its efficiency in bulk is drastically decreased since itsthermal instability limits the possibility to reach high molecular weight poly(L-lactide) (PL-LA). Under optimum conditions,PL-LA chains with average molecular weight up to 10,000 g.mol-1 have been obtained within 15 minutes and interestinglycharacterized by very narrow polydispersity indices. Compared to PL-LA conventionally prepared with stannousoctoate as catalyst, the thermal stability proved remarkably enhanced when the ROP was promoted by 1.
机译:L,L-丙交酯(L-LA)的开环聚合(ROP)已使用醇(甲醇或苄醇)和1,3,4-三苯基-4,5-二氢-1H-1进行了批量研究在一定的温度范围和醇与1的摩尔比范围内,分别用作引发剂和非有机金属催化剂的1,2,4-三唑-5亚烷基卡宾。尽管已知1可以在90℃下完全控制L-LA在溶液中的聚合,但是由于其热不稳定性限制了达到高分子量聚(L-丙交酯)(PL-LA)的可能性,因此其整体效率大大降低。在最佳条件下,可以在15分钟内获得平均分子量高达10,000 g.mol-1的PL-LA链,并具有很窄的多分散性指数。与传统的以辛二酸锡为催化剂制备的PL-LA相比,当ROP升高1时,热稳定性得到显着提高。

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