Design and prompt synthesis of a hydrazone-linked covalent organic framework with binding pockets for lanthanides: Luminescent pH and ratiometric temperature sensing

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL
Himanshi Bhambri, Sanjay Mandal
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Abstract

Focusing on the exceptional traits of a highly functionalized, flexible, and yet infrequent hydrazone linkages, a new covalent organic framework, namely BTD, is synthesized by the fast crystallization technique within 1.5 h. Extensive characterization by various spectroscopic and microscopic techniques, powder X-ray diffraction, and computational simulation confirms its purity, structural features, and porous nature. The framework is locked due to the presence of secondary interactions such as intralayer (N···H-O and C-H···O=C), interlayer (N-H···O) H-bonding as well as π-π stacking, which provides in-plane rigidness in the staggered AB type stacking of layers. These strong interactions can be the possible reason for the prompt crystallization of BTD. The dual proton donor and acceptor sites offered by functionalized hydrazone linkage in BTD lead to the wide-range, colorimetric, luminescent detection of hydrogen ion concentration. Its luminescence is highest at pH 4 but quenched in strong basic medium (pH 13). Furthermore, to embark upon the characteristics of hydrazone connectivity and anchored functional groups (carbonyl and hydroxy), the trivalent lanthanides are incorporated onto the decorated pockets yielding Tb@BTD and Eu@BTD. Utilizing the remarkable thermal detection features of lanthanide-decorated COFs, the ratiometric temperature detection studies are performed in the aqueous and methanolic slurries. The computed relative sensitivity values for Tb@BTD and Eu@BTD are: 1.404 % K-1 and 1.118 % K-1 at 333 K in water and 2.73 % K-1 and 2.29 % K-1 at 313 K in methanol, respectively. For noting the utility of both COFs in real environmental conditions, the change in luminescence is studied in the temperature range of 308-320 K. With a quenching of 22%, Eu@BTD proves to be a better candidate to work for effective luminescent thermometric applications under physiological conditions.
设计和快速合成含镧系元素结合袋的腙连接共价有机骨架:发光pH值和比例温度传感
针对高功能化、柔性和不常见的腙键的特殊特性,采用快速结晶技术在1.5小时内合成了一种新的共价有机骨架,即BTD。通过各种光谱和微观技术、粉末x射线衍射和计算模拟进行了广泛的表征,证实了其纯度、结构特征和多孔性。由于二级相互作用的存在,如层内(N··h·O和C·h·O=C)、层间(N- h·O)氢键以及π-π堆叠,框架被锁定,这为交错AB型层堆叠提供了面内刚度。这些强相互作用可能是BTD迅速结晶的原因。在BTD中,功能化的腙键提供了双质子供体和受体位点,从而实现了氢离子浓度的宽范围、比色、发光检测。其发光在ph4时最高,在强碱介质(ph13)中猝灭。此外,为了利用腙连接和锚定官能团(羰基和羟基)的特性,将三价镧系元素结合到修饰的口袋中,产生Tb@BTD和Eu@BTD。利用镧系装饰COFs显著的热检测特性,在水浆和甲醇浆中进行了比例温度检测研究。计算得到的Tb@BTD和Eu@BTD的相对灵敏度值分别为:水中333 K时为1.404 % K-1和1.118 % K-1,甲醇中313 K时为2.73% K-1和2.29% K-1。为了说明这两种COFs在实际环境条件下的效用,研究了308-320 K温度范围内的发光变化。由于猝灭率为22%,Eu@BTD被证明是生理条件下有效发光测温应用的更好候选材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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