4.6 Article

2,5-Diisopropenylthiophene by Suzuki-Miyaura cross-coupling reaction and its exploitation in inverse vulcanization: a case study

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RSC ADVANCES
卷 12, 期 15, 页码 8924-8935

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra00654e

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  1. Compagnia di San Paolo (Turin, Italy) [IDROL 20583]
  2. Italian Ministry for Universities and Research (MUR) [2020TS9LXS]

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A novel thiophene derivative, 2,5-diisopropenylthiophene (DIT), was synthesized by Suzuki-Miyaura cross-coupling reaction (SMCCR) and used as a comonomer in the inverse vulcanization (IV) process with waste elemental sulfur to obtain sulfur-rich polymers called inverse vulcanized polymers (IVPs) with high refractive index. The design of DIT was aimed at promoting the IV process and enhancing the refractive index of the resulting IVPs. A series of S-r-DIT copolymers with varying sulfur content were synthesized by adjusting the S/DIT feed ratio, and the main chemical-physical features of the new IVPs were characterized.
A novel thiophene derivative, namely 2,5-diisopropenylthiophene (DIT) was synthetized by Suzuki-Miyaura cross-coupling reaction (SMCCR). The influence of reaction parameters, such as temperature, solvent, stoichiometry of reagents, role of the base and reaction medium were thoroughly discussed in view of yield optimization and environmental impact minimization. Basic design of experiment (DoE) and multiple linear regression (MLR) modeling methods were used to interpret the obtained results. DIT was then employed as a comonomer in the copolymerization with waste elemental sulfur through a green process, inverse vulcanization (IV), to obtain sulfur-rich polymers named inverse vulcanized polymers (IVPs) possessing high refractive index (n approximate to 1.8). The DIT comonomer was purposely designed to (i) favor the IV process owing to the high reactivity of the isopropenyl functionalities and (ii) enhance the refractive index of the ensuing IVPs owing to the presence of the sulfur atom itself and to the high electronic polarizability of the pi-conjugated thiophene ring. A series of random sulfur-r-diisopropenylthiophene (S-r-DIT) copolymers with sulfur content from 50 up to 90 wt% were synthesized by varying the S/DIT feed ratio. Spectroscopic, thermal and optical characterizations of the new IVPs were carried out to assess their main chemical-physical features.

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