首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Positive shift in corrole redox potentials leveraged by modest beta-CF3-substitution helps achieve efficient photocatalytic C-H bond functionalization by group 13 complexes
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Positive shift in corrole redox potentials leveraged by modest beta-CF3-substitution helps achieve efficient photocatalytic C-H bond functionalization by group 13 complexes

机译:符合适度的β-CF3替代物利用的腐蚀氧化还原电位的正偏移有助于通过第13组复合物实现高效的光催化C-H键官能化

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Tris- and tetrakis-beta-trifluoromethylated gallium (3CF(3)-Ga, 4CF(3)-Ga) and aluminum (3CF(3)-Al, 4CF(3)-Al) corrole systems were synthesized by a facile "one-pot" approach from the respective tri- and tetra-iodo starting compounds using the FSO2CF2CO2Me reagent. The isolated 5,10,15-(tris-pentafluorophenyl)corrole-based compounds set the groundwork for another important beta-substituent study in inorganic photocatalysis. As seen previously, -CF3 group substitution leads to red shifts in both the absorption and emission spectra compared to their unsubstituted counterparts (X. Zhan, et al., Inorg. Chem., 2019, 58, 6184-6198). All CF3-substituted corrole complexes showed strong fluorescence; 3CF(3)-Al possessed the highest fluorescence quantum yield (0.71) among these compounds. The photocatalytic production of bromophenol by way of these photosensitizing complexes was studied demonstrating that tris-trifluoromethylation is an important substitution class, especially when Ga3+ is present (experimental TON value in parentheses): 3CF(3)-Ga (192) > 4CF(3)-Ga (146) > 3CF(3)-Al (130) > 4CF(3)-Al (56) > 1-Ga (43) > 1-Al (18). The catalytic performance (turn-over number, TON) for benzylbromide formation (from toluene) was found to be: 3CF(3)-Ga (225) > 1-Ga (138) > 3CF(3)-Al (130) > 4CF(3)-Ga (126) > 1-Al (95) > 4CF(3)-Al (89); in these trials, benzaldehyde was also detected as a product in which 3CF(3)-Ga outperforms the other compounds (TON = 109). The tetra-CF3-substituted 4CF(3)-Ga and 4CF(3)-Al species exhibit a dramatic formal positive shift of 116 mV and 126 mV per [CF3] group, respectively, compared to the unsubstituted parent species 1-Ga and 1-Al. However, the absorbance values (lambda(abs) = 400 nm) of these corrole complexes (all equally concentrated: 4.0 x 10(-6) M) were 3CF(3)-Al (0.23) > 3CF(3)-Ga (0.22) > 1-Al (0.21) > 1-Ga (0.20) > 4CF(3)-Al (0.19) > 4CF(3)-Ga (0.15), which helps rationalize why 3CF(3)-Ga performs the best among these catalysts. These new
机译:三 - 和四-β-三氟甲基化镓(3CF(3)-Ga,4CF(3)-Ga)和铝(3CF(3)-Al,4CF(3)-Al)corrole系统由一个浅显合成“一一锅”从相应的三 - 和四方法碘开始使用FSO2CF2CO2Me试剂的化合物。所述分离5,10,15-(三 - 五氟苯基)基于corrole化合物设置在无机光催化另一个重要的β-取代基的研究的基础。如前面所看到的,-CF 3基团的取代导致在吸收和发射光谱两者红移相比,其未取代的对应物(X.詹,等人,Inorg化学杂志,2019年,58,6184-6198)。所有CF3取代corrole络合物表现出较强的荧光; 3CF(3)-Al具有这些化合物当中的最高荧光量子产率(0.71)。光催化生产由这些光敏复合物的方式溴苯酚进行了研究表明三 - 三氟甲基化是一个重要的替代类,特别是当GA3 +的情况下(在括号中的实验TON值):3CF(3)-Ga(192)> 4CF(3 )-Ga(146)> 3CF(3)-Al(130)> 4CF(3)-Al(56)> 1 - 镓(43)> 1 - 铝(18)。为苄基的形成(从甲苯中)的催化能力(翻转数,TON)被发现是:3CF(3)-Ga(225)> 1 - 镓(138)> 3CF(3)-Al(130)> 4CF(3)-Ga(126)> 1 - 铝(95)> 4CF(3)-Al(89);在这些试验中,苯甲醛也检测为其中3CF(3)-Ga优于其它化合物(TON = 109)的产物。该四-CF 3 - 取代的4CF(3)-Ga和4CF(3)-Al物种表现出116 mV的戏剧性形式正移和每[CF 3]组相比,分别以未取代的母体物种1 - 镓126 mV与1-A1中。然而,该吸光值(拉姆达(绝对压力)= 400nm)的这些corrole复合物(都同样浓缩:4.0×10(-6)M)分别3CF(3)-Al(0.23)> 3CF(3)-Ga( 0.22)> 1 - 铝(0.21)> 1 - 镓(0.20)> 4CF(3)-Al(0.19)> 4CF(3)-Ga(0.15),这有助于合理化为什么3CF(3)-Ga执行最佳这些催化剂之一。这些新的

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