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Bioimaging,as a powerful and helpful tool,which allows people to investigate deeply within living organisms,has contributed a lot for both clinical theranostics and scientific research.Pure organic room temperature phosphorescence(RTP)materials with the unique features of ultralong luminescence lifetime and large Stokes shift,can efficiently avoid biological autofluorescence and scattered light through a time-resolved imaging modality,and thus are attracting increasing attention.This review classifies pure organic RTP materials into three categories,including small molecule RTP materials,polymer RTP materials and supramolecular RTP materials,and summarizes the recent advances of pure organic RTP materials for bioimaging applications. 相似文献
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钯 铂 卟啉络合物在室温下发射长寿命 (ms)、长波长的光 ,这些特点使其在生物分析方面成为有用的探针。本文综述了该探针在光免疫标记、肿瘤诊断、DNA测定、生物传感器及其它方面的研究进展。引用文献 4 3篇 相似文献
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Lili Huang Chen Qian Prof. Zhiyong Ma 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(52):11914-11930
This Minireview summarizes the recent progress of stimuli-responsive purely organic phosphorescence materials. Organic phosphorescence is closely related to the intermolecular interactions, because such interactions are beneficial to promote spin orbital coupling (SOC) and boost intersystem cross (ISC) efficiency and finally are conducive to satisfactory phosphorescence. It is found that the intermolecular interactions, which are essential for organic phosphorescence, are easily disturbed by external stimuli such as mechanical force, photon, acid, chemical vapor, leading to the luminescence change. According to this principle, various purely organic phosphorescence materials sensitive to external stimuli have been developed. This Minireview categorizes reported stimuli-responsive purely organic phosphorescence materials on the basis of different stimuli, including mechanochromism, mechanoluminescence, photoactivity, acid-responsiveness and other stimuli. Some prospective strategies for constructing stimuli-responsive purely organic phosphorescence molecules are provided. 相似文献
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Lingyun Lou Tianqi Xu Yuzhan Li Changli Zhang Bochun Wang Xusheng Zhang Hean Zhang Yuting Qiu Junyan Yang Dong Wang Hui Cao Wanli He Zhou Yang 《Molecules (Basel, Switzerland)》2022,27(19)
Pure organic room-temperature phosphorescence (RTP) materials built upon noncovalent interactions have attracted much attention because of their high efficiency, long lifetime, and stimulus-responsive behavior. However, there are limited reports of noncovalent RTP materials because of the lack of specific design principles and clear mechanisms. Here, we report on a noncovalent material prepared via facile grinding that can emit fluorescence and RTP emission differing from their components’ photoluminescent behavior. Exciplex can be formed during the preparation process to act as the minimum emission unit. We found that H-bonds in the RTP system provide restriction to nonradiative transition but also enhance energy transformation and energy level degeneracy in the system. Moreover, water-stimulated photoluminescent ink is produced from the materials to achieve double-encryption application with good resolution. 相似文献
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Hui Li Huanhuan Li Wu Wang Ye Tao Shuang Wang Qingqing Yang Yunbo Jiang Chao Zheng Wei Huang Runfeng Chen 《Angewandte Chemie (International ed. in English)》2020,59(12):4756-4762
Purely organic materials showing room temperature phosphorescence (RTP) and ultralong RTP (OURTP) have recently attracted much attention. However, it is challenging to integrate circularly polarized luminescence (CPL) into RTP/OURTP. Here, we show a strategy to realize CPL‐active OURTP (CP‐OURTP) by binding an achiral phosphor group directly to the chiral center of an ester chain. Engineering of this flexible chiral chain enables efficient chirality transfer to carbazole aggregates, resulting in strong CP‐OURTP with a lifetime of over 0.6 s and dissymmetry factor of 2.3×10?3 after the conformation regulation upon photo‐activation. The realized CP‐OURTP is thus stable at room temperature but can be deactivated quickly at 50 °C to CP‐RTP with high CPL stability during the photo‐activation/thermal‐deactivation cycles. Based on this extraordinary photo/thermal‐responsive and highly reversible CP‐OURTP/RTP, a CPL‐featured lifetime‐encrypted combinational logic device has been successfully established. 相似文献
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MXene是一类新型的二维过渡金属碳化物和氮化物的总称,通式为Mn + 1XnTx(n = 1~3),其中M为前过渡金属元素,X为碳或氮元素,T指键合在该材料表面的氟基、羟基或氧基等活性官能团。该类材料具有超薄的结构和出色的物理化学(电子、光学、磁性等)特性,从而吸引了各领域研究人员的广泛兴趣。目前,MXene在生物医学领域的应用逐渐拓展。这主要是由于其大的表面积和在近红外区域的强吸收,加之其可以通过容易的表面修饰与多种分子或者纳米颗粒结合。在这篇综述中,我们总结了MXene在生物医学应用中的最新进展。文章首先介绍MXene的相关制备方法和表面改性手段;之后重点围绕其独特的理化性质,依次介绍该材料在抗菌材料、生物成像、肿瘤诊断治疗和生物传感等生物医学领域中的应用进展;文章最后总结讨论了MXene在生物医学应用方面面临的挑战和新机遇。预期超薄MXene及精巧设计的纳米复合物将成为多种生物医学应用的最有吸引力的生物相容性无机纳米平台之一。 相似文献
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Dr. Xiaolei Cai Prof. Bin Liu 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(25):9952-9970
The concept of aggregation-induced emission (AIE) has opened new opportunities in many research fields. Motivated by the unique feature of AIE fluorogens (AIEgens), during the past decade, many AIE molecular probes and AIE nanoparticle (NP) probes have been developed for sensing, imaging and theranostic applications with excellent performance outperforming conventional fluorescent probes. This Review summarizes the latest advancement of AIE molecular probes and AIE NP probes and their emerging biomedical applications. Special focus is to reveal how the AIE probes are evolved with the development of new multifunctional AIEgens, and how new strategies have been developed to overcome the limitations of traditional AIE probes for more translational applications via fluorescence imaging, photoacoustic imaging and image-guided photodynamic/photothermal therapy. The outlook discusses the challenges and future opportunities for AIEgens to advance the biomedical field. 相似文献
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The concept of aggregation‐induced emission (AIE) has opened new opportunities in many research fields. Motivated by the unique feature of AIE fluorogens (AIEgens), during the past decade, many AIE molecular probes and AIE nanoparticle (NP) probes have been developed for sensing, imaging and theranostic applications with excellent performance outperforming conventional fluorescent probes. This Review summarizes the latest advancement of AIE molecular probes and AIE NP probes and their emerging biomedical applications. Special focus is to reveal how the AIE probes are evolved with the development of new multifunctional AIEgens, and how new strategies have been developed to overcome the limitations of traditional AIE probes for more translational applications via fluorescence imaging, photoacoustic imaging and image‐guided photodynamic/photothermal therapy. The outlook discusses the challenges and future opportunities for AIEgens to advance the biomedical field. 相似文献
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Ehsan Hamzehpoor Dmitrii F. Perepichka 《Angewandte Chemie (International ed. in English)》2020,59(25):9977-9981
We report a series of highly emissive azatriangulenetrione (TANGO) solids in which the luminescent properties are controlled by engineering the molecular packing by adjusting the steric size of substituents. The co‐alignment of “phosphorogenic” carbonyl groups within the π‐stacks results in an almost pure triplet emission in HTANGO, TCTANGO, TBTANGO and TITANGO, while their rotation by ≈60° in the sterically hindered tBuTANGO leads to an almost pure singlet emission. Despite strong π‐interactions, aggregation‐induced quenching and triplet–triplet annihilation are avoided in HTANGO and TCTANGO which display efficient phosphorescence in the solid state. To our knowledge, HTANGO with the solid‐state phosphorescence quantum yield of 42 % at room temperature is the most efficient phosphor composed of the 1st/2nd raw elements only. 相似文献
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Tailoring Intermolecular Interactions for Efficient Room‐Temperature Phosphorescence from Purely Organic Materials in Amorphous Polymer Matrices 下载免费PDF全文
Sungbaek Seo Jaehun Jung Prof. Dr. Jinsang Kim 《Angewandte Chemie (International ed. in English)》2014,53(42):11177-11181
Herein we report a rational design strategy for tailoring intermolecular interactions to enhance room‐temperature phosphorescence from purely organic materials in amorphous matrices at ambient conditions. The built‐in strong halogen and hydrogen bonding between the newly developed phosphor G1 and the poly(vinyl alcohol) (PVA) matrix efficiently suppresses vibrational dissipation and thus enables bright room‐temperature phosphorescence (RTP) with quantum yields reaching 24 %. Furthermore, we found that modulation of the strength of halogen and hydrogen bonding in the G1–PVA system by water molecules produced unique reversible phosphorescence‐to‐fluorescence switching behavior. This unique system can be utilized as a ratiometric water sensor. 相似文献
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Yufei Yang Fucheng Gao Yandong Wang Hui Li Jie Zhang Zhiwei Sun Yanyan Jiang 《Molecules (Basel, Switzerland)》2022,27(23)
The activity levels of key substances (metal ions, reactive oxygen species, reactive nitrogen, biological small molecules, etc.) in organisms are closely related to intracellular redox reactions, disease occurrence and treatment, as well as drug absorption and distribution. Fluorescence imaging technology provides a visual tool for medicine, showing great potential in the fields of molecular biology, cellular immunology and oncology. In recent years, organic fluorescent probes have attracted much attention in the bioanalytical field. Among various organic fluorescent probes, fluorescent organic small molecule probes (FOSMPs) have become a research hotspot due to their excellent physicochemical properties, such as good photostability, high spatial and temporal resolution, as well as excellent biocompatibility. FOSMPs have proved to be suitable for in vivo bioimaging and detection. On the basis of the introduction of several primary fluorescence mechanisms, the latest progress of FOSMPs in the applications of bioimaging and detection is comprehensively reviewed. Following this, the preparation and application of fluorescent organic nanoparticles (FONPs) that are designed with FOSMPs as fluorophores are overviewed. Additionally, the prospects of FOSMPs in bioimaging and detection are discussed. 相似文献
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通过多种重原子微扰剂和实验条件的选择,成功地实现了C6SCl在数种基质上的RTP发射。发现Pb(Ⅱ)盐是这种RTP发射的最有效的外部重原子微扰剂。在滤纸基质上,以1mol/L Pb(Ac)_2作重原子微扰剂获得了强度高且信/背比亦高的RTP信号,λ_(ex)/λ_(em)=320/496nm。0.2μl点样体积中,C6SCl含量在4~200pmol范围内与RTP信号强度呈良好的线性关系。 相似文献
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本文研究了吲哚的无保护流体室温燐光(NP-RTP)性质。基于NP-RTP建立起来的分析方法已直接用于鱼中吲哚的测定。方法的线性范围为1.0×10-7~7.0×10-6mol/L,相对标准偏差为2.1%~3.4%。本方法无须保护性介质而仅以KI为重原子微扰剂、Na2SO3为除氧剂即可。0.60 mol/L KI、2.0×10-3mol/L Na2SO3和pH 8.6为方法的最佳测定条件。 相似文献
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Chao Shi Deshuang Tu Qi Yu Hua Liang Yahong Liu Zhihong Li Prof. Dr. Hong Yan Prof. Dr. Qiang Zhao Prof. Dr. Wei Huang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(50):16550-16557
New iridium tetrazolate complexes containing o‐, m‐, or p‐carboranyl substitution in different positions of a phenylpyridine ligand have been prepared. The carborane isomers and the effect of their substitution position in the tuning of optical properties have been examined. The neutral complexes with the carboranyl substituent on the phenyl ring in meta position relative to the metal exhibit redshifted emission bands in contrast to blueshifts for those with carboranyl in para position. All cationic complexes display evidently blueshifted dual‐peak emission compared with the carborane‐free complex (c‐ TZ ) with a broad single‐peak emission. Introduction of carborane leads to a blueshift over 70 nm relative to c‐ TZ . Carboranes also significantly improve phosphorescence efficiency (ΦP) and lifetime (τ), that is, ΦP=0.64 versus 0.21 (c‐ TZ ) and τ=880 ns versus 241 ns (c‐ TZ ). The unique hydrophilic nido‐carborane‐based IrIII complex nido‐o‐ 1 shows the largest phosphorescence efficiency (abs ΦP=0.57) among known water‐soluble iridium complexes, long emission lifetime (τ=4.38 μs), as well as varying emission efficiency and lifetime with O2 content in aqueous solution. Therefore, nido‐o‐ 1 has been used as an excellent oxygen‐sensitive phosphor for intracellular O2 sensing and hypoxia imaging. 相似文献