Investigating structure-fluorescence properties of imidazole fused tetraphenylethylene AIEgens: Reversible mechanofluorochromism and polymer matrix controlled fluorescence tuning

CrystEngComm ◽  
2021 ◽  
Author(s):  
Palaniyappan Nagarasu ◽  
Anu Kundu ◽  
Vijay Thiruvenkatam ◽  
Raghavaiah Pallepogu ◽  
Philip Philip Anthony ◽  
...  
Keyword(s):  
Solid State ◽  
Polymer Matrix ◽  
Fluorescence Properties ◽  
Stimuli Responsive ◽  
Fluorescent Properties ◽  
Imidazole Derivatives

A series of stimuli-responsive AIEgens of tetraphenylethyelene (TPE) fused Imidazole derivatives (1-7) were synthesized and explored their substituents controlled fluorescent properties in the solid state. The structure of the synthesized...

Solid-state Reversible Optical Switch Based on Two Dendritic Molecules with dual sensitivity of mechanochromism and photochromism

2021 ◽  
Author(s):  
Yuhui Yang ◽  
Zhe He ◽  
Junzhao He ◽  
Yuqing Li ◽  
Yilong Chen ◽  
...  
Keyword(s):  
Solid State ◽  
Polymer Matrix ◽  
Optical Switch ◽  
New Method ◽  
Photochromic Molecules ◽  
Conformational Freedom

Efficient isomerization of photochromic molecules requires conformational freedom and is often limited to the solution or polymer matrix. Thus, developing a new method to improve photochromism in the solid state...

Carbazole-modified thiazolo[3,2-c][1,3,5,2]oxadiazaborinines exhibiting aggregation-induced emission and mechanofluorochromism

2021 ◽  
Author(s):  
Mykhaylo A. Potopnyk ◽  
Mykola Kravets ◽  
Roman Luboradzki ◽  
Dmytro Volyniuk ◽  
Volodymyr Sashuk ◽  
...  
Keyword(s):  
Solid State ◽  
Fluorescence Properties ◽  
Aggregation Induced Emission ◽  
Donor Acceptor ◽  
Solid State Fluorescence ◽  
Active Donor

Two novel AIE-active donor–acceptor organoboron complexes with a carbazole donor unit are developed and their morphology-dependent solid-state fluorescence properties are established.

scholarly journals Redox-State Dependent Spectroscopic Properties of Porous Organic Polymers Containing Furan, Thiophene, and Selenophene

2017 ◽  
Vol 70 (11) ◽  
pp. 1227 ◽  
Author(s):  
Carol Hua ◽  
Stone Woo ◽  
Aditya Rawal ◽  
Floriana Tuna ◽  
James M. Hook ◽  
...  
Keyword(s):  
Solid State ◽  
Redox State ◽  
Spectroscopic Properties ◽  
Structural Features ◽  
Organic Polymers ◽  
Stimuli Responsive ◽  
Porous Organic Polymers ◽  
Paramagnetic Resonance ◽  
Responsive Materials ◽  
State Dependent

A series of electroactive triarylamine porous organic polymers (POPs) with furan, thiophene, and selenophene (POP-O, POP-S, and POP-Se) linkers have been synthesised and their electronic and spectroscopic properties investigated as a function of redox state. Solid state NMR provided insight into the structural features of the POPs, while in situ solid state Vis-NIR and electron paramagnetic resonance spectroelectrochemistry showed that the distinct redox states in POP-S could be reversibly accessed. The development of redox-active porous organic polymers with heterocyclic linkers affords their potential application as stimuli responsive materials in gas storage, catalysis, and as electrochromic materials.

Molecular Motion Analysis of 5CB in PDLCs Using Solid-State 13C NMR Relaxation Spectroscopy

1993 ◽  
Vol 47 (7) ◽  
pp. 933-941 ◽  
Author(s):  
Karen L. Buchert ◽  
Jack L. Koenig ◽  
Shi-Qing Wang ◽  
John L. West
Keyword(s):  
Liquid Crystal ◽  
Solid State ◽  
Polymer Matrix ◽  
Nmr Relaxation ◽  
Domain Size ◽  
Chemical Structures ◽  
Similar Chemical ◽  
Polymer Dispersed ◽  
Submicron Droplets ◽  
Significant Change

In samples of polymer-dispersed liquid crystals (PDLCs), submicron droplets of liquid crystal reside within a polymer matrix. By the use of the cross polarization technique for solid-state 13C NMR spectroscopy, the NMR spectrum of the liquid crystal can be obtained without interference from the polymer spectrum, even though the two materials have some similar chemical structures. Both 13C T1 and 13C T1 ρ relaxation experiments were performed on a PDLC system of 5CB in epoxy as a function of 5CB domain size. The 13C T1 relaxation constants and the localized motions they measure showed no significant change over the liquid crystal domain size studied. However, the 13C T1 ρ relaxation constants and the segmental motions of molecules they measure revealed a significant change over the liquid crystal domain size studied. Therefore, the 13C T1 ρ values can be used to determine the change in mobility of the molecular segments of the SCB molecules resulting from increased interaction between the liquid crystal and the polymer matrix and to further understand the importance of the molecular motions of the liquid crystal in the switching phenomenon for PDLC materials.

Ultra-thin Solid-State Li-Ion Electrolyte Membrane Facilitated by a Self-Healing Polymer Matrix

2015 ◽  
Vol 27 (43) ◽  
pp. 6922-6927 ◽  
Author(s):  
Justin M. Whiteley ◽  
Philip Taynton ◽  
Wei Zhang ◽  
Se-Hee Lee
Keyword(s):  
Solid State ◽  
Polymer Matrix ◽  
Self Healing ◽  
Electrolyte Membrane ◽  
Li Ion

Reversible stimuli-responsive luminescence of bimetallic cuprous complexes based on NH-deprotonated 3-(2′-pyridyl)pyrazole

2021 ◽  
Author(s):  
Yang Tong ◽  
xingwei Chen ◽  
Li-Hua He ◽  
Jing-Lin Chen ◽  
Sui-Jun Liu ◽  
...  
Keyword(s):  
Solid State ◽  
Stimuli Responsive ◽  
State Luminescence ◽  
Color Regulation

Color regulation of solid-state luminescence is desirable and challenging. Herein we report two new three- and four-coordinate bimetallic cuprous complexes 1 and 2, which bear a NH-deprotonated 3-(2′-pyridyl)pyrazole adopting monoanionic...

scholarly journals Redox-triggered switching in three-dimensional covalent organic frameworks

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Chao Gao ◽  
Jian Li ◽  
Sheng Yin ◽  
Junliang Sun ◽  
Cheng Wang
Keyword(s):  
Solid State ◽  
Three Dimensional ◽  
Molecular Switches ◽  
Pore Channel ◽  
Pore Surface ◽  
Stimuli Responsive ◽  
Conversion Yield ◽  
Responsive Materials ◽  
Reversible Transformation ◽  
Internal Pore

Abstract The tuning of molecular switches in solid state toward stimuli-responsive materials has attracted more and more attention in recent years. Herein, we report a switchable three-dimensional covalent organic framework (3D COF), which can undergo a reversible transformation through a hydroquinone/quinone redox reaction while retaining the crystallinity and porosity. Our results clearly show that the switching process gradually happened through the COF framework, with an almost quantitative conversion yield. In addition, the redox-triggered transformation will form different functional groups on the pore surface and modify the shape of pore channel, which can result in tunable gas separation property. This study strongly demonstrates 3D COFs can provide robust platforms for efficient tuning of molecular switches in solid state. More importantly, switching of these moieties in 3D COFs can remarkably modify the internal pore environment, which will thus enable the resulting materials with interesting stimuli-responsive properties.

Triphenylamine-based stimuli-responsive solid state fluorescent materials

2020 ◽  
Vol 44 (21) ◽  
pp. 8680-8696 ◽  
Author(s):  
Parthsarathy Gayathri ◽  
Mehboobali Pannipara ◽  
Abdullah G. Al-Sehemi ◽  
Savarimuthu Philip Anthony
Keyword(s):  
Solid State ◽  
Molecular Engineering ◽  
Stimuli Responsive ◽  
Fluorescent Materials

Molecular engineering of triphenylamine (TPA) units produced multi-stimuli-responsive solid state fluorescent materials.

scholarly journals Characterization of steady-state fluorescence properties of polystyrene latex spheres using off- and online spectroscopic methods

2018 ◽  
Vol 11 (7) ◽  
pp. 3987-4003 ◽  
Author(s):  
Tobias Könemann ◽  
Nicole J. Savage ◽  
J. Alex Huffman ◽  
Christopher Pöhlker
Keyword(s):  
Steady State ◽  
Polystyrene Latex ◽  
Fluorescence Properties ◽  
Minor Role ◽  
Spectroscopic Techniques ◽  
Fluorescent Properties ◽  
Qualitative Comparison ◽  
Steady State Fluorescence ◽  
Research Communities ◽  
Latex Spheres

Abstract. Fluorescent dyed polystyrene latex spheres (PSLs) are commonly used for characterization and calibration of instruments detecting fluorescence signals from particles suspended in the air and other fluids. Instruments like the Ultraviolet Aerodynamic Particle Sizer (UV-APS) and the Waveband Integrated Bioaerosol Sensor (WIBS) are widely used for bioaerosol research, but these instruments present significant technical and physical challenges requiring careful characterization with standard particles. Many other research communities use flow cytometry and other instruments that interrogate fluorescence from individual particles, and these also frequently rely on fluorescent PSLs as standards. Nevertheless, information about physical properties of commercially available PSLs provided by each manufacturer is generally proprietary and rarely available, making their use in fluorescence validation and calibration very difficult. This technical note presents an overview of steady-state fluorescence properties of fluorescent and non-fluorescent PSLs, as well as of polystyrene-divinylbenzene (PS-DVB) particles, by using on- and offline spectroscopic techniques. We show that the “fluorescence landscape” of PSLs is more complex than the information typically provided by manufacturers may imply, especially revealing multimodal emission patterns. Furthermore, non-fluorescent PSLs also exhibit defined patterns of fluorescent emission originating from a mixture of polystyrene and detergents, which becomes a crucial point for fluorescence threshold calibrations and qualitative comparison between instruments. By comparing PSLs of different sizes, but doped with the same dye, changes in emission spectra from bulk solutions are not immediately obvious. On a single-particle scale, however, fluorescence intensity values increase with increasing particle size. No significant effect in the fluorescence signatures was detectable by comparing PSLs in dry vs. wet states, indicating that solvent water may only play a minor role as a fluorescence quencher. Because information provided by manufacturers of commercially available PSLs is generally very limited, we provide the steady-state excitation–emission matrices (EEMs) of PSLs as open-access data within the Supplement. Detergent and solvent effects are also discussed in order to provide information not available elsewhere to researchers in the bioaerosol and other research communities. These data are not meant to serve as a fundamental library of PSL properties because of the variability of fluorescent properties between batches and as a function of particle aging and agglomeration. The data presented, however, provide a summary of spectral features which are consistent across these widely used fluorescent standards. Using these concepts, further checks will likely be required by individual researchers using specific lots of standards.

Sign in / Sign up

Export Citation Format

Share Document