含硼酸基团的发光铱(III)配合物:碳水化合物的潜在传感器

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Rahad Rahman, Nurul H Quazi, Keith Forrest White, Nicolau Saker Neto, Yuning Hong, Marcel Maeder, David John Wilson, Peter Barnard
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引用次数: 0

摘要

已经制备了一个8个Ir(III)配合物家族,其形式为[Ir(X)2(L)]+(其中X = 2-苯基吡啶,1-苯基吡唑,2-苯基苯并噻唑或1-苯基苯并唑和L = 2-(吡唑-1-基)吡啶在吡啶环或吡唑环的第4位被硼酸基取代),作为碳水化合物检测的潜在发光传感器。这些配合物已经通过1h和13C NMR, HRMS和x射线晶体学对配合物11,12,14和18进行了充分的表征。光致发光pH滴定研究表明,配合物11-14在4.9-5.3的pKa范围内,配合物15-18在6.4-7.8的pKa范围内,硼酸基团转化为硼酸阴离子形式,硼酸阴离子的形成伴随着这些化合物的光致发光特性的显著变化。在葡萄糖和果糖存在的情况下,对复合物进行了类似的pH滴定研究,通过光致发光滴定数据估计了这些糖与复合物之间通过环硼酸酯形成的结合常数;与葡萄糖相比,果糖的结合明显更强。有趣的是,环硼酸酯的形成导致配合物12、13、16和17的发光强度一致降低,而配合物11、14、15和18的发光强度增强。理论计算支持实验观察。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Luminescent Iridium(III) Complexes Bearing Boronic Acid Groups: Potential Sensors for Carbohydrates
A family of eight Ir(III) complexes of the form [Ir(X)2(L)]+ (where X = 2-phenylpyridine, 1-phenylpyrazole, 2-phenylbenzothiazole or 1-phenylindazole and L = 2-(pyrazole-1-yl)pyridine substituted with a boronic acid group at position four of either the pyridyl or the pyrazole ring) have been prepared as potential luminescent sensors for carbohydrate detection. These complexes have been fully characterised via1H and 13C NMR, HRMS and for complexes 11, 12, 14, and 18 by X-ray crystallography. Photoluminescent pH titration studies showed conversion of the boronic acid group to the boronate anionic form occurred within the pKa range of 4.9-5.3 for complexes 11-14 and 6.4-7.8 for complexes 15-18, with formation of the boronate anion being accompanied by significant changes in the photoluminescence emission properties of these compounds. Similar pH titration studies were undertaken for the complexes in the presence of glucose and fructose sugars, with the binding constants between these sugars and the complexes via cyclic boronate ester formation estimated from the photoluminescent titration data; significantly stronger binding was observed for fructose compared to glucose. Interestingly, the formation of the cyclic boronate ester results in a consistent decrease in the emission intensity for complexes 12, 13, 16, and 17 while complexes 11, 14, 15, and 18 showed enhanced luminescence. Theoretical calculations support the experimental observations.
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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