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CONFORMATIONS OF TRICYANOFURAN-TYPE METASTABLE-STATE PHOTOACIDS
Title
CONFORMATIONS OF TRICYANOFURAN-TYPE METASTABLE-STATE PHOTOACIDS.
Creator
Arias, Juan E, Chumbimuni-Torres, Karin Y., University of Central Florida
Abstract / Description
Tricyanofuran-type metastable-state photoacids, relative newcomers to the field of photochromism, outperform traditional light-controlled molecular switches in regards to applicability in biological systems. In a preliminary attempt to understand the underlying processes that govern these compounds, this thesis project establishes the isomeric identity of an unsubstituted tricyanofuran-type metastable-state photoacid, referred to as TCF 1 in this work. Two-dimensional nuclear magnetic...
Show moreTricyanofuran-type metastable-state photoacids, relative newcomers to the field of photochromism, outperform traditional light-controlled molecular switches in regards to applicability in biological systems. In a preliminary attempt to understand the underlying processes that govern these compounds, this thesis project establishes the isomeric identity of an unsubstituted tricyanofuran-type metastable-state photoacid, referred to as TCF 1 in this work. Two-dimensional nuclear magnetic resonance experiments are employed to experimentally determine the presence and identity of the open-form TCF 1 isomers. Electronic structure calculations are then used to provide quantitative insight into the experimental results. Experiment and theory show that four out of eight possible open-form isomers exist in solution. To validate the information obtained theoretically, the calculation methodologies are tested against experimental chemical shifts. The impressive agreement with the experiments gives credibility to the picture painted by the theoretical models.
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Date Issued
2019
Identifier
CFH2000470, ucf:45707
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFH2000470
Ultrafast Mechanisms of Nonlinear Refraction and Two-photon Photochromism
Title
Ultrafast Mechanisms of Nonlinear Refraction and Two-photon Photochromism.
Creator
Zhao, Peng, Hagan, David, Vanstryland, Eric, Christodoulides, Demetrios, Hernandez, Florencio, University of Central Florida
Abstract / Description
Derived from a material's third-order nonlinearity, nonlinear refraction (NLR) occurs at any wavelength in any material, and may exhibit noninstantaneous dynamics depending on its physical origins. The main subject of this dissertation is to investigate the underlying mechanisms responsible for the NLR response in different phases of matter, e.g. liquids, gases, and semiconductors, by extensively using our recently developed ultrafast Beam Deflection (BD) technique. An additional subject...
Show moreDerived from a material's third-order nonlinearity, nonlinear refraction (NLR) occurs at any wavelength in any material, and may exhibit noninstantaneous dynamics depending on its physical origins. The main subject of this dissertation is to investigate the underlying mechanisms responsible for the NLR response in different phases of matter, e.g. liquids, gases, and semiconductors, by extensively using our recently developed ultrafast Beam Deflection (BD) technique. An additional subject includes the characterization of a novel two-photon photochromic molecule.In molecular liquids, the major nonlinear optical (NLO) response can be decomposed into a nearly instantaneous bound-electronic NLR (Kerr effect), originating from the real part the electronic second hyperpolarizability, ?, and noninstantaneous mechanisms due to nuclear motions. By adopting the methodology previously developed for carbon disulfide (CS2), we have measured the NLO response functions of 23 common organic solvents, providing a database of magnitudes and temporal dynamics of each mechanism, which can be used for predicting the outcomes of any other NLR related experiments such as Z-scan. Also, these results provide insight to relate solvent nonlinearities with their molecular structures as well as linear polarizability tensors. In the measurements of air and gaseous CS2, coherent Raman excitation of many rotational states manifests as revivals in the transient NLR, from which we identify N2, O2 and two isotopologues of CS2, and unambiguously determine the dephasing rate, and rotational and centrifugal constants of each constituent. Using the revival signal as a self-reference, ? is directly measured for CS2 molecules in gas phase, which coincides with the ? determined from liquid phase measurements when including the Lorentz-Lorenz local field correction. In semiconductors, the Kerr effect dominates the NLR in the sub-gap regime. Here, we primarily focus on investigating the dispersion of nondegenerate (ND) NLR, namely the refractive index change at frequency ?_a due to the presence of a beam at frequency ?_b. The magnitude and sign of the ND-NLR coefficient n_2 (?_a;?_b ) are determined for ZnO, ZnSe and CdS over a broad spectral range for different values of nondegeneracy, which closely follows our earlier predictions based on nonlinear Kramers-Kronig relations. In the extremely nondegenerate case, n_2 (?_a;?_b ) is positively enhanced near the two-photon absorption (2PA) edge, suggesting applications for nondegenerate all-optical switching. Additionally, n_2 (?_a;?_b ) exhibits a strong anomalous nonlinear dispersion within the ND-2PA spectral region, providing a large phase modulation of a femtosecond pulse with bandwidth centered near the zero-crossing frequency. Another subject of this dissertation is the characterization of a spiro-type two-photon photochromic molecule, in which F(&)#246;rster resonance energy transfer (FRET) is utilized to activate the ring-opening effect from a 2PA-donor chromophore. Evidence of energy transfer is observed via fluorescence measurements of the quantum yield, excitation spectra and anisotropy. The absorption and lifetime of the open form are measured in a dye-doped sol-gel matrix. Transient absorption measurements indicate both ring opening and closing occurs on a several picosecond time scale along with multiple transient photoproducts, from which a high FRET efficiency is measured in agreement with theoretical predictions. This efficient 2PA-FRET photochrome may be implemented into photonic devices such as optical memories. However, with a relatively small open-form absorption cross section and significant ring closing, the photochrome may not be viable for enhancing nonlinear absorption in applications such as optical limiting.
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Date Issued
2016
Identifier
CFE0006517, ucf:51370
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0006517
SIMULATION OF PHOTOCHROMIC COMPOUNDS USING DENSITY FUNCTIONAL THEORY METHODS
Title
SIMULATION OF PHOTOCHROMIC COMPOUNDS USING DENSITY FUNCTIONAL THEORY METHODS.
Creator
Patel, Pansy, Masunov, Artem, University of Central Florida
Abstract / Description
This Thesis describes the systematic theoretical study aimed at prediction of the essential properties for the functional organic molecules that belong to diarylethene (DA) family of compounds. Diarylethenes present the distinct ability to change color under the influence of light, known as photochromism. This change is due to ultrafast chemical transition from open to closed ring isomers (photocyclization). It can be used for optical data storage, photoswitching, and other photonic...
Show moreThis Thesis describes the systematic theoretical study aimed at prediction of the essential properties for the functional organic molecules that belong to diarylethene (DA) family of compounds. Diarylethenes present the distinct ability to change color under the influence of light, known as photochromism. This change is due to ultrafast chemical transition from open to closed ring isomers (photocyclization). It can be used for optical data storage, photoswitching, and other photonic applications. In this work we apply Density Functional Theory methods to predict 6 of the related properties: (i) molecular geometry; (ii) resonant wavelength; (iii) thermal stability; (iv) fatigue resistance; (v) quantum yield and (vi) nanoscale organization of the material. In order to study sensitivity at diode laser wavelengths, we optimized geometry and calculated vertical absorption spectra for a benchmark set of 28 diarylethenes. Bond length alternation (BLA) parameters and maximum absorption wavelengths (λmax) are compared to the data presently available from X-ray diffraction and spectroscopy experiments. We conclude that TD-M05/6-31G*/PCM//M05-2X/6-31G*/PCM level of theory gives the best agreement for both the parameters. For our predictions the root mean square deviation (RMSD) are below 0.014 Å for the BLAs and 25 nm for λmax. The polarization functions in the basis set and solvent effects are both important for this agreement. Next we consider thermal stability. Our results suggest that UB3LYP and UM05-2X functionals predict the activation barrier for the cycloreversion reaction within 3-4 kcal/mol from experimental value for a set of 7 photochromic compounds. We also study thermal fatigue, defined as the rate of undesirable photochemical side reactions. In order to predict the kinetics of photochemical fatigue, we investigate the mechanism of by-product formation. It has been established experimentally that the by-product is formed from the closed isomer; however the mechanism was not known. We found that the thermal by-product pathway involves the bicyclohexane (BCH) ring formation as a stable intermediate, while the photochemical by-product formation pathway may involve the methylcyclopentene diradical (MCPD) intermediate. At UM05-2X/6-31G* level, the calculated barrier between the closed form and the BCH intermediate is 51.2 kcal/mol and the barrier between the BCH intermediate and the by-product 16.2 kcal/mol. Next we investigate two theoretical approaches to the prediction of quantum yield (QY) for a set of 14 diarylethene derivatives at the validated M05-2X/6-31G* theory level. These include population of ground-state conformers and location of the pericycylic minimum on the potential energy surface 2-A state. Finally, we investigate the possibility of nanoscale organization of the photochromic material based on DNA template, as an alternative to the amorphous polymer matrix. Here we demonstrate that Molecular Dynamic methods are capable to describe the intercalation of π-conjugated systems between DNA base pairs and accurately reproduced the available photophysical properties of these nanocomposites. In summary, our results are in good agreement with the experimental data for the benchmark set of molecules we conclude that Density Functional Theory methods could be successfully used as an important component of material design strategy in prediction of accurate molecular geometry, absorption spectra, thermal stability of isomers, fatigue resistance, quantum yield of photocyclization and photophysical properties of nanocomposites.
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Date Issued
2010
Identifier
CFE0003136, ucf:48633
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0003136
TWO-PHOTON 3D OPTICAL DATA STORAGE VIA FLUORESCENCE MODULATION OF FLUORENE DYES BY PHOTOCHROMIC DIARYLETHENES
Title
TWO-PHOTON 3D OPTICAL DATA STORAGE VIA FLUORESCENCE MODULATION OF FLUORENE DYES BY PHOTOCHROMIC DIARYLETHENES.
Creator
Corredor, Claudia, Belfield, Kevin D., University of Central Florida
Abstract / Description
Three-dimensional (3D) optical data storage based on two-photon processes provides highly confined excitation in a recording medium and a mechanism for writing and reading data with less cross talk between multiple memory layers, due to the quadratic dependence of two photon absorption (2PA) on the incident light intensity. The capacity for highly confined excitation and intrinsic 3D resolution affords immense information storage capacity (up to 1012 bits/cm3). Recently, the use of...
Show moreThree-dimensional (3D) optical data storage based on two-photon processes provides highly confined excitation in a recording medium and a mechanism for writing and reading data with less cross talk between multiple memory layers, due to the quadratic dependence of two photon absorption (2PA) on the incident light intensity. The capacity for highly confined excitation and intrinsic 3D resolution affords immense information storage capacity (up to 1012 bits/cm3). Recently, the use of photochromic materials for 3D memory has received intense interest because of several major advantages over current optical systems, including their erasable/rewritable capability, high resolution, and high sensitivity. This work demonstrates a novel two-photon 3D optical storage system based on the modulation of the fluorescence emission of a highly efficient two-photon absorbing fluorescent dye (fluorene derivative) and a photochromic compound (diarylethene). The feasibility of using efficient intermolecular Förster Resonance Energy Transfer (RET) from the non-covalently linked two-photon absorbing fluorescent fluorene derivative to the photochromic diarylethene as a novel read-out method in a two-photon optical data storage system was explored. For the purpose of the development of this novel two-photon 3D optical storage system, linear and two-photon spectroscopic characterization of commercial diarylethenes in solution and in a polymer film and evidence of their cyclization (O→C) and cycloreversion (C→O) reactions induced by two-photon excitation were undertaken. For the development of a readout method, Resonance Energy Transfer (RET) from twophoton absorbing fluorene derivatives to photochromic compounds was investigated under one and two-photon excitation. The Förster's distances and critical acceptor concentrations were determined for non-bound donor-acceptor pairs in homogeneous molecular ensembles. To the best of my knowledge, modulation of the two-photon fluorescence emission of a dye by a photochromic diarylethene has not been reported as a mechanism to read the recorded information in a 3D optical data storage system. This system was demonstrated to be highly stable and suitable for recording data in thick storage media. The proposed RET-based readout method proved to be non-destructive (exhibiting a loss of the initial fluorescence emission less than 20% of the initial emission after 10,000 readout cycles). Potential application of this system in a rewritable-erasable optical data storage system was proved. As part of the strategy for the development of diarylethenes optimized for 3D optical data storage, derivatives containing π-conjugated fluorene molecules were synthesized and characterized. The final part of this reasearch demonstrated the photostability of fluorine derivatives showing strong molecular polarizability and high fluorescence quantum yields. These compounds are quite promising for application in RET-based two-photon 3D optical data storage. Hence, the photostability of these fluorene derivatives is a key parameter to establish, and facilitates their full utility in critical applications.
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Date Issued
2007
Identifier
CFE0001662, ucf:47210
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0001662
TWO-PHOTON CROSS SECTION ENHANCEMENT OF PHOTOCHROMIC COMPOUNDS FOR USE IN 3D OPTICAL DATA STORAGE
Title
TWO-PHOTON CROSS SECTION ENHANCEMENT OF PHOTOCHROMIC COMPOUNDS FOR USE IN 3D OPTICAL DATA STORAGE.
Creator
Luchita, Gheorghe, Belfield, Kevin, University of Central Florida
Abstract / Description
Rewritable photochrome-based 3D optical data storage requires photochromic molecules with high two-photon absorption (2PA) cross sections. Currently, the low value of two-photon absorption cross sections of existing photochromes makes them unsuitable for practical application in 3D data storage. Worldwide attempts to increase the cross section of photochromic molecules by altering the chemical structure have yielded poor results. In this work, two ways to increase the two-photon absorption...
Show moreRewritable photochrome-based 3D optical data storage requires photochromic molecules with high two-photon absorption (2PA) cross sections. Currently, the low value of two-photon absorption cross sections of existing photochromes makes them unsuitable for practical application in 3D data storage. Worldwide attempts to increase the cross section of photochromic molecules by altering the chemical structure have yielded poor results. In this work, two ways to increase the two-photon absorption cross sections of photochromes were investigated. In the first method, partial success demonstrated by extending the conjugation of a photochromic molecule, a high two-photon absorption cross section of the closed form isomer and high photoconversion to the closed form were realized. At the same time, a decrease in photoswitching quantum yield and low photoconversion to open form was observed. A discussion is provided to explain the results, suggesting that the proposed method of extending the conjugation may not solve the problem. For this reason a new method for effective two-photon absorption cross section enhancement of photochromes was proposed. As a proof of principle, a new two-photon absorbing dye with a hydrogen bonding moiety was synthesized and used for the formation of supramolecular structures with a photochromic compound. Theoretical reasoning and experimental demonstration of energy transfer from the dye to the photochrome under one and two-photon excitation confirmed the practical value of the method. The effects of a 2PA dye on the photochromic properties of a diarylethene were investigated using a model compound to simplify data analysis. Formation of supramolecular structures was revealed using 1H NMR spectroscopic methods. The model compound, having the same hydrogen bonding moiety as 2PA dye, has been demonstrated to bind with photochrome molecules at very low concentrations. Photochromic properties of 2,3-bis(2,4,5-trimethyl-3-thienyl)maleimide, including conversions at the photostationary state, extinction coefficients, photoisomerization reaction rates and quantum yields, were shown to be affected by hydrogen bonding with the model compound - 2,6-bis-(acetamido)pyridine. The extent of this change was determined and discussed, demonstrating a balanced supramolecular strategy to modulate photochemical and photophysical properties of this important class of photochromic material.
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Date Issued
2011
Identifier
CFE0003928, ucf:48695
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0003928
Metastable-State Photoacids: Synthesis, Properties, and Applications
Title
Metastable-State Photoacids: Synthesis, Properties, and Applications.
Creator
Patel, Parth, Chumbimuni Torres, Karin, Hernandez, Florencio, Santra, Swadeshmukul, Beazley, Melanie, Lee, Woo Hyoung, University of Central Florida
Abstract / Description
Reversible photochromic compounds have the ability to reversibly change its color when it absorbs photons of a particular wavelength. This process of color change is a consequence of structural changes within the compound, such as cis-trans photo-isomerization. Some examples of photochromic compounds are spiropyrans, spirooxazines, diarylethenes and azobenzenes. These compounds have been extensively studied for decades, and are used in various applications such as biomedicine, chemical...
Show moreReversible photochromic compounds have the ability to reversibly change its color when it absorbs photons of a particular wavelength. This process of color change is a consequence of structural changes within the compound, such as cis-trans photo-isomerization. Some examples of photochromic compounds are spiropyrans, spirooxazines, diarylethenes and azobenzenes. These compounds have been extensively studied for decades, and are used in various applications such as biomedicine, chemical sensors and harvesting solar energy. However, majority of photochromic compounds are initially activated by ultraviolet (UV) light. The use of UV light is harmful for biological applications and photo-degrade the compound over repeated use. To overcome these limitations, a new class of reversible photochromic compound was introduced, called metastable-state photoacid (mPAH). In brief, mPAH is a photochromic compound which can photo-dissociate its protons under visible light and can thermally re-capture the released protons efficiently in the dark. Based on this unique property, in this research, we (1) synthesized different mPAH, and (2) studied and characterized their physicochemical (acidity, kinetics, and optical) properties. Additionally, we (3) applied different visible light activated mPAHs towards light controllable polymeric-based ion-selective optodes for detection of calcium ions and sodium ions, and modulate fluorescence with pH. The research presented herein opens new avenues towards the synthesis of mPAH derivatives and could be applied to any proton-transfer process related applications which requires wireless controllability with high sensitivity.
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Date Issued
2019
Identifier
CFE0007849, ucf:52769
Format
Document (PDF)
PURL
http://purl.flvc.org/ucf/fd/CFE0007849