Dinesh G. Patel

ORCID: 0000-0003-0733-5383
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Photochromic and Fluorescence Chemistry
  • Conducting polymers and applications
  • Organic Electronics and Photovoltaics
  • Organic Light-Emitting Diodes Research
  • Crystallography and molecular interactions
  • Photochemistry and Electron Transfer Studies
  • Porphyrin and Phthalocyanine Chemistry
  • Photoreceptor and optogenetics research
  • Metal-Organic Frameworks: Synthesis and Applications
  • Bioactive Compounds and Antitumor Agents
  • Molecular Sensors and Ion Detection
  • Structural and Chemical Analysis of Organic and Inorganic Compounds
  • GaN-based semiconductor devices and materials
  • Perovskite Materials and Applications
  • Crystal structures of chemical compounds
  • Organic and Inorganic Chemical Reactions
  • Industrial Vision Systems and Defect Detection
  • Adaptive optics and wavefront sensing
  • Supramolecular Self-Assembly in Materials
  • Thermal properties of materials
  • Nonlinear Optical Materials Studies
  • Spectroscopy and Quantum Chemical Studies
  • Axial and Atropisomeric Chirality Synthesis

Pennsylvania State University
2014-2024

University of Aberdeen
2021

Hazleton Eye Specialists
2014-2015

University of Florida
2011-2013

University at Buffalo, State University of New York
2012-2013

Seattle University
2011

University of Washington
2005-2011

University of Alberta
2010

University of Victoria
2010

We report on the comparison of electronic and photophysical properties a series related donor–acceptor–donor oligomers incorporating previously known 2H-benzo[d][1,2,3]triazole (BTz) moiety as acceptor recently reported BTzTD acceptor, hybrid BTz 2,1,3-benzothiadiazole (BTD). Although often implied in polymer literature that has good character, we show this is best described weak acceptor. present electrochemical, computational, evidence supporting our assertion strong electron while...

10.1021/ja207978v article EN Journal of the American Chemical Society 2012-01-31

Heteroannulated benzothiadizole acceptors in donor–acceptor polymers.

10.1039/c4mh00102h article EN Materials Horizons 2014-08-06

Herein we report the synthesis and characterization of light responsive metal organic framework (MOF) single crystals containing photochromic diarylethene 1,2-bis(2,5-dimethyl-thien-3-yl)perfluorocyclopentene. Polarized microscopy on indicates that photochrome is preferentially aligned along c-axis host.

10.1039/c3cc44119a article EN Chemical Communications 2013-01-01

Stabilization of unfavorable rotational isomers within the nanoporous crystalline matrix reduces useful lifetime this photo-switchable material.

10.1039/c5nj01718a article EN New Journal of Chemistry 2015-09-21

The synthesis and characterization of novel photochromic diarylethene-based linkers for use in metal–organic frameworks is described including crystal structure analysis nearly all reaction intermediates.

10.1039/c3cc49666j article EN Chemical Communications 2014-01-01

Tailor-made additives, which are molecules that share the same molecular structure as a parent molecule with only slight structural variations, have previously been demonstrated useful means to control crystallization dynamics in solution. For example, tailor-made additives can be added solutions of crystallizing alter crystal growth rate, size, and shape. We apply this strategy predictably morphology bulk-heterojunction (BHJ) photovoltaic cells. Through use an asymmetric oligomer...

10.1021/am301944g article EN ACS Applied Materials & Interfaces 2012-12-03

The effects of solution-state dielectric and intermolecular interactions on the degree charge separation in metastable spirooxazine photomerocyanines (PMCs) is investigated. We report first X-ray diffraction (XRD) analyses an open form, a photomerocyanine, class photochromic molecules two derivatives: spiro[azahomoadamantane-isoquinolinoxazine] (1) spiro[azahomoadamantane-phenanthrolinoxazine] (2). Using results XRD analysis photomerocyanine forms, conjunction with computation,...

10.1021/ja100238h article EN Journal of the American Chemical Society 2010-08-23

Abstract Polymer photovoltaic devices commonly suffer from low power conversion efficiencies despite the potential for much higher performance. Here we apply a recently reported system creating chemically fixed polymer p‐i‐n junction to devices. Both single‐component and blended donor/acceptor are fabricated tested. We study during charging find that changes in light dark current characteristics consistent with formation of active material. While overall performance these systems need...

10.1002/adfm.200700824 article EN Advanced Functional Materials 2008-04-17

The single crystals of a closed form spirooxazine spiro[azahomoadamantane-isoquinolinoxazine] were found for the first time to undergo photocoloration processes consistent with photochromism in crystalline phase.

10.1039/b417026a article EN Chemical Communications 2005-01-01

The chemistry of electron deficient π-acceptors offers unique challenges in the rational design and synthesis organic dyes for use solar cells. We have synthesized 2-cyano-2-(3-cyano-4-((E)-4-(dibutylamino)styryl)-5,5-dimethylfuran-2(5H)-ylidene)ethanoic acid (2), a dye containing an carboxylated version strongly withdrawing TCF group by way stepwise isolation 2,5-dihydro-2-imino-4,5,5-trimethylfuran-3-carbonitrile (5), previously only available as intermediate via microwave chemistry. this...

10.1039/c0jm03774e article EN Journal of Materials Chemistry 2011-01-01

We report on the synthesis of a polyfluorene derivative, PFO(X), with furan pendant groups capable Diels–Alder crosslinking maleimide containing small molecule passive crosslinker (PC) and red emitting donor–acceptor–donor dopant molecule, bE-BTD(X). It was initially intended that blend these three components would afford system where concentration could be increased to point complete energy transfer from host polymer emissive achieved. Because such systems often suffer quenching shifts in...

10.1039/c2jm14591j article EN Journal of Materials Chemistry 2012-01-01

We report the synthesis and characterization of 2,3-bis(5-iodo-2-methylthiophen-3-yl)naphthalene-1,4-dione its ring-closed isomer.

10.1039/d4ce00112e article EN cc-by-nc CrystEngComm 2024-01-01

Abstract We report the synthesis of a 3‐ethylhexyloxy substituted poly( meta ‐phenylene), EHO‐PMP that shows absorption and solid state photoluminescence exclusively in UV region electromagnetic spectrum with an emission maximum 345 nm. Computational analysis model oligomers by DFT methods indicates is wide bandgap polymer HOMO being localized on dimeric (biphenyl) unit LUMO more delocalized. The energy LUMO, however, suggests inefficient electron injection would occur from currently...

10.1002/polb.22224 article EN Journal of Polymer Science Part B Polymer Physics 2011-03-01

Organic photochromic molecules including diarylethenes are of particular interest for their numerous potential applications high-density optical data storage and light-activated switches. In this report, we examined the temperature dependence light-drive photocyclization reaction in a classic diarylethene. The steady-state populations were monitored spectroscopically by dependent situ photocrystallography, latter being first reported example technique. observed decrease population with...

10.1021/jp512488q article EN The Journal of Physical Chemistry A 2015-01-09

Diarylethene photochromes show promise for use in advanced organic electronic and photonic materials with burgeoning considerations biological applications; however, these compounds typically require UV light photoswitching at least one direction, thus limiting their appeal. We here introduce a naphthoquinone-based diarylethene that switches between open closed forms visible light. The synthesis of this quinone relies on Suzuki methodology, allowing the inclusion functional groups not...

10.1021/acs.joc.9b02632 article EN The Journal of Organic Chemistry 2020-01-03

Photochromic compounds have a lengthy history of study and profusion applications that stand to gain from these studies. Among the classes photochromic compounds, diarylethenes show desirable properties including high fatigue resistance thermal stability, thus meeting some most important criteria necessary enter realm practical applications. Recently, containing quinone functionalities demonstrated interesting optical solid-state properties. When properly interfaced with suitable electron...

10.3390/molecules25112630 article EN cc-by Molecules 2020-06-05

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDissociation of molecular iodine by excited iodine(2P1/2) atomsD. Patel and David J. BenardCite this: Phys. Chem. 1985, 89, 15, 3274–3276Publication Date (Print):July 1, 1985Publication History Published online1 May 2002Published inissue 1 July 1985https://pubs.acs.org/doi/10.1021/j100261a021https://doi.org/10.1021/j100261a021research-articleACS PublicationsRequest reuse permissionsArticle Views114Altmetric-Citations4LEARN ABOUT THESE...

10.1021/j100261a021 article EN The Journal of Physical Chemistry 1985-07-01

The title tri-phenyl-amine derivative, C24H17Cl2N, featuring a 3,5-di-chloro-1,1'-biphenyl moiety has been synthesized and structurally characterized. mol-ecular structure shows rotations of the phenyl rings in range 37-40° from amine plane. In crystal, mol-ecules inter-act by van der Waals inter-actions.

10.1107/s2414314621010166 article EN cc-by IUCrData 2021-10-13

Organic photochromic molecules including diarylethenes are of particular interest for their potential applications in fields high density optical data storage and light-activated switches, among many others. However, one the limitations diarylethene-based systems has been low photoconversion observed neat single crystals which is often less than 20%. The conversion typically believed to be result screening effects photoisomerized at surface absorb incident light preventing full isomerization...

10.1107/s2053273314092328 article EN Acta Crystallographica Section A Foundations and Advances 2014-08-05
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