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Data on the synthesis and mechanical characterization of polysiloxane-based urea-elastomers prepared from amino-terminated polydimethylsiloxanes and polydimethyl-methyl-phenyl-siloxane-copolymers

机译:由氨基封端的聚二甲基硅氧烷和聚二甲基-甲基-苯基-硅氧烷共聚物制备的基于聚硅氧烷的脲弹性体的合成和机械表征数据

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摘要

This article contains data on the synthesis and mechanical characterization of polysiloxane-based urea-elastomers (PSUs) and is related to the research article entitled “Influence of PDMS molecular weight on transparency and mechanical properties of soft polysiloxane-urea-elastomers for intraocular lens application” (Riehle et al., 2018) [1]. These elastomers were prepared by a two-step polyaddition using the aliphatic diisocyanate 4,4′-Methylenbis(cyclohexylisocyanate) (H12MDI), a siloxane-based chain extender 1,3-Bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane (APTMDS) and amino-terminated polydimethylsiloxanes (PDMS) or polydimethyl-methyl-phenyl-siloxane-copolymers (PDMS-Me,Ph), respectively. (More details about the synthesis procedure and the reaction scheme can be found in the related research article (Riehle et al., 2018) [1]).Amino-terminated polydimethylsiloxanes with varying molecular weights and PDMS-Me,Ph-copolymers were prepared prior by a base-catalyzed ring-chain equilibration of a cyclic siloxane and the endblocker APTMDS. This DiB article contains a procedure for the synthesis of the base catalyst tetramethylammonium-3-aminopropyl-dimethylsilanolate and a generic synthesis procedure for the preparation of a PDMS having a targeted number average molecular weight M¯n of 3000 g mol−1. Molecular weights and the amount of methyl-phenyl-siloxane within the polysiloxane-copolymers were determined by 1H NMR and 29Si NMR spectroscopy. The corresponding NMR spectra and data are described in this article.Additionally, this DiB article contains processed data on in line and off line FTIR-ATR spectroscopy, which was used to follow the reaction progress of the polyaddition by showing the conversion of the diisocyanate. All relevant IR band assignments of a polydimethylsiloxane-urea spectrum are described in this article.Finally, data on the tensile properties and the mechanical hysteresis-behaviour at 100% elongation of PDMS-based polyurea-elastomers are shown in dependence to the PDMS molecular weight.
机译:本文包含有关基于聚硅氧烷的脲弹性体(PSU)的合成和机械表征的数据,并且与题为“ PDMS分子量对用于人工晶状体的软聚硅氧烷-脲弹性体的透明度和机械性能的影响有关的研究文章(Riehle et al。,2018)[1]。通过使用脂肪族二异氰酸酯4,4'-亚甲基双(环己基异氰酸酯)(H12MDI),硅氧烷基扩链剂1,3-双(3-氨基丙基)-1,1,3, 3-四甲基二硅氧烷(APTMDS)和氨基末端的聚二甲基硅氧烷(PDMS)或聚二甲基-甲基-苯基-硅氧烷共聚物(PDMS-Me,Ph)。 (有关合成步骤和反应方案的更多详细信息,请参见相关研究文章(Riehle等,2018)[1])。制备了具有不同分子量的氨基封端的聚二甲基硅氧烷和PDMS-Me,Ph共聚物首先通过环硅氧烷和封端剂APTMDS的碱催化的环链平衡。该DiB文章包含碱催化剂四甲基铵-3-氨基丙基-二甲基硅烷醇酸酯的合成方法,以及制备具有目标数均分子量的PDMS的通用合成方法。 M ¯ n 等于3000 g mol -1 。用 1 1 H NMR和 29 Si NMR光谱法测定聚硅氧烷共聚物中的分子量和甲基-苯基-硅氧烷的含量。相应的NMR光谱和数据在本文中进行了描述。此外,该DiB文章还包含在线和离线FTIR-ATR光谱处理的数据,该数据用于通过显示二异氰酸酯的转化来跟踪加聚反应的进展。本文描述了聚二甲基硅氧烷-脲光谱的所有相关IR波段分配。最后,显示了PDMS基聚脲-弹性体在100%伸长率下的拉伸性能和机械滞后行为的数据。

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