Department of Chemistry, Institute for Coatings and Surface Chemistry, Niederrhein University of Applied Sciences, Adlerstr. 1, 47798, Krefeld, Germany.
Chemistry. 2021 Mar 1;27(13):4297-4301. doi: 10.1002/chem.202005076. Epub 2021 Feb 15.
NIR and UV exposure of systems comprising upconversion nanoparticles (UCNP) based on NaYF :Tm/Yb@NaYF , a sensitizer absorbing either in the blue or UV region, and an onium salt with weak coordinating anion resulted in formation of conjugate acid (con-H ). That was namely Ivocerin (di(4-methoxybenzoyl)diethylgermane), ITX (2-iso-propyl thioxanthone), anthracene, pyrene, rubrene, camphore quinone, and a strong fluorescent coumarin (1,1,6,6,8-pentamethyl-2,3,5,6-tetrahyhdro-1H,4H-11-oxa-3a-aza-benzo[de]anthracene-10-one). Quantification occurred by treatment with Rhodamine B lactone whose color switched to intensive red after photolytic formation of con-H . Exposure with a NIR laser at 980 nm resulted in less con-H compared to 395 nm where all sensitizers absorb radiation. UCNP did not mainly interfered formation of con-H . The different rates obtained in both experiments responsibly explain the failure and success to initiate polymerization of epoxides applying ether 980 nm or 395 nm excitation, respectively.
上转换纳米粒子(UCNP)基 NaYF:Tm/Yb@NaYF 的系统在近红外(NIR)和紫外(UV)暴露下,吸收剂在蓝区或 UV 区吸收,以及具有弱配位阴离子的翁盐导致形成共轭酸(con-H)。即 Ivocerin(二(4-甲氧基苯甲酰基)二乙基锗烷)、ITX(2-异丙基噻吨酮)、蒽、芘、并五苯、樟脑醌和强荧光香豆素(1,1,6,6,8-五甲基-2,3,5,6-四氢-1H,4H-11-氧杂-3a-氮杂苯并[de]蒽-10-酮)。通过用罗丹明 B 内酯处理进行定量,其在光解形成 con-H 后颜色变为强烈的红色。与所有吸收剂吸收辐射的 395nm 相比,980nm 的近红外激光照射导致形成的 con-H 较少。UCNP 并没有主要干扰 con-H 的形成。这两种实验中获得的不同速率分别负责解释分别用 980nm 或 395nm 激发醚引发环氧化物聚合的失败和成功。