Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus U.A.B., 08193 Bellaterra, Barcelona, Spain.
Molecules. 2020 Mar 7;25(5):1210. doi: 10.3390/molecules25051210.
High boron content systems were prepared by the peripheral functionalisation of 1,3,5-triphenylbenzene (TPB) and octavinylsilsesquioxane (OVS) with two different anionic boron clusters: -dodecaborate (B) and cobaltabisdicarbollide (COSAN). TPB was successfully decorated with three cluster units by an oxonium ring-opening reaction, while OVS was bonded to eight clusters by catalysed metathesis cross-coupling. The resulting compounds were spectroscopically characterised, and their solution-state photophysical properties analysed. For TPB, the presence of COSAN dramatically quenches the fluorescence emission (λ = 369 nm; Φ = 0.8%), while B-substituted TPB shows an appreciable emission efficiency (λ = 394 nm; Φ = 12.8%). For octasilsesquioxanes, the presence of either COSAN or B seems to be responsible for ∼80 nm bathochromic shift with respect to the core emission, but both cases show low emission fluorescence (Φ = 1.4-1.8%). In addition, a remarkable improvement of the thermal stability of OVS was observed after its functionalisation with these boron clusters.
高硼含量体系是通过 1,3,5-三苯基苯(TPB)和辛基乙烯基倍半硅氧烷(OVS)与两种不同的阴离子硼簇:-十二硼酸盐(B)和钴双碳硼烷(COSAN)的外围功能化制备的。TPB 通过氧鎓开环反应成功地修饰了三个簇单元,而 OVS 通过催化的复分解交叉偶联键合到八个簇上。所得化合物进行了光谱表征,并分析了它们在溶液状态下的光物理性质。对于 TPB,COSAN 的存在极大地猝灭了荧光发射(λ=369nm;Φ=0.8%),而 B 取代的 TPB 则显示出可观的发射效率(λ=394nm;Φ=12.8%)。对于八硅倍半氧烷,COSAN 或 B 的存在似乎导致相对于核发射的约 80nm 红移,但两种情况的荧光发射都很低(Φ=1.4-1.8%)。此外,在硼簇功能化后,OVS 的热稳定性得到了显著提高。