Collagen is an important structural protein in living organisms and plays an indispensable role in connecting cells and tissues, such as in musculature, bone, and ligament. The stability and conformation of collagen are, however, strongly influenced by ambient temperature and constitutes an interesting subject of study. Thermally induced conformation change of collagen has been investigated by techniques such as differential scanning calorimetry (DSC) and second harmonic generation. DSC is a powerful method in uncovered important thermal dynamics properties including phase change, enthalpy, and thermal stability of the collagen. However, due to its collective nature, no localized information can be found. For comparison, second harmonic generation, which reflects structural symmetry, can be combined with laser scanning microscopy to investigate localized variation. It has been shown in previous studies that the thermal stability of collagen is strongly influenced by the water content within collagen. For comparison, we are investigating the conformational change of collagen under a vacuum stat with second harmonic microscopy so as to isolate environmental effects, particularly those from water and oxygen. In this way, we have found the conformational change of collagen takes place at a much higher temperature and activation energy. Additionally, the high spatial resolution achieved also allows many further possibilities.

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Thesis (Ph. D.)--University of Texas at Austin, 2000. / Vita. Includes bibliographical references (leaves 72-82). Available also in a digital version from Dissertation Abstracts.

Thesis (Ph. D.)--University of Chicago, Department of Chemistry, 2002. / Includes bibliographical references. Also available on the Internet.

Thesis (Ph.D)--Physics, Georgia Institute of Technology, 2010. / Committee Chair: Rick Trebino; Committee Member: Ahmet Erbil; Committee Member: John Buck; Committee Member: Stephen Ralph; Committee Member: Zhigang Jiang. Part of the SMARTech Electronic Thesis and Dissertation Collection.

Optical imaging has been developed quickly in the past decades because it has become an important research tool in biology, biochemistry, and biomedical sciences. Coherence domain optical imaging is one of the well developed optical imaging modalities, as it provides high resolution and long penetration depth. In this dissertation, we will report our work on development of molecular contrast in coherence domain optical imaging. In order to image important molecules which are poor fluorophores, we developed a high resolution molecular imaging technique, pump-probe optical coherence microscopy (PPOCM), which does not rely on fluorescent tags. PPOCM is the fusion of Pump-Probe spectroscopy and optical coherence microscopy (OCM). We have demonstrated the prototype system on a fixed human skin sample containing a nodular melanoma. The results indicate that PPOCM can clearly provide strong contrast between the melanotic and amelanotic regions. This technique can be applied to early diagnosis of melanoma and the mapping of tumor margins during excision. It also can be extended to any biological chromophore with a known absorption spectrum and sufficient concentration. In order to differentiate further multiple chromophores, we developed a spectrally resolved two color pump-probe Optical Coherence Microscopy (SRPPOCM). We showed the prototype system on a red hair and a black hair. Our preliminary results show that the SRPPOCM technique could provide a contrast between pheomelanin and eumelanin. This technique could be used potentially as a clinical tool for diagnosing different progression stages of melanoma. This technique could also be applied to differentiate other mixed chromophores. Second harmonic optical coherence tomography (SHOCT) is non-linear high resolution optical molecular imaging modality which is widely used in non-centrosymmetric material. However, depth ambiguity is associated with SHOCT in tissue sample because forward generated second harmonic signal does not correctly report where the second harmonic signal is generated. We studied the feasibility of collecting the backward generated second harmonic signal from nanocrystals through a Second Harmonic Optical Coherence Tomography in Fourier domain. The preliminary result shows that we can collect backward generated second harmonic signal from nanocrystals which indicates that this technique could suppress the depth ambiguity.

The linear and nonlinear optical response of plasmon hybridized systems is the subject of study of this thesis. Plasmonic silver nanoprisms are able to confine light to a sub-wavelength volume, which provides local field enhancement. This confined field is promising for achieving an enhanced nonlinear optical response. For many of plasmon nanoparticles, however, the plasmonic resonance is not at the near-infrared wavelengths of a Ti:Sapphire laser, the most common source used for ultra-fast measurements. To achieve resonance at these wavelengths, a tuning mechanism is required. The plasmon hybridization between silver nanoprisms and a thin gold film provides this tuning mechanism, which allows for enhanced optical second harmonic generation. Overlapping the plasmon resonance of the system with excitation source, by varying the spacer layer between the nanoprisms and the gold film, enhances the second harmonic counts by approximately three orders of magnitude. The finite-difference time-domain calculations agree to within a factor of two with the experimental findings in terms of the predicted enhancement factor. This plasmon hybridization approach is promising for future applications, including enhanced multi-photon lithography and nonlinear sensing using metal nanoparticles. / Graduate

This Thesis is concerned with the prediction, synthesis, characterization and testing of inorganic materials for Second Harmonic Generation (SHG). Chapter One describes the fundamentals of non-linear optics, and poses the problems, and some of their solutions which confront the synthetic chemist and the theoretical prediction of the second order hyperpolarizability constant β using CNDOVSB calculations. Chapter Two describes the design, implementation and calibration of an apparatus for measurements of the second harmonic generating efficiency of solids based on the Kurtz powder technique, and a solvatochromic method for the determination of β. Novel compounds with potential chirality due to atropisomerism, asymmetric octahedral structures, and asymmetric tetrahedral symmetry of metal centers are discussed in Chapters Three to Five. Chapter Three surveys the use of pentane-2,4-dionato- ligands and their coordination compounds as possible NLO active materials. The single crystal X-ray structures of bis(triphenylphosphine)(4-nitrobenzoylacetonato)palladium(II) tetrafluoroborate and tris(triphenylphosphine)[3-(2,4-dinitrophenyl)-pentane-2,4-dionato]palladium(II) tetrafluoroborate were determined. Chapter Four describes the syntheses, characterization and SHG properties of trans-β-ionylidenecyanoacetic acid (2-cyano-3-methyl-5-(2,6,6-trimethyl-l-cyclohexen-1- yl)-2,4-pentadienoic acid) and some of its metal and non-metal salts. Chapter Five describes the synthesis, characterization and second harmonic generation properties of some platinum(II) and palladium(II) complexes of β- ionylidenecyanoacetic acid. Chapter Six describes the use of conventional asymmetric carbon centers to introduce chirality into centrosymmetric compounds. The chiral compound (L)-N-[2-cyano- 3-methyl-5-(2,6,6-trimethyl-1 -cyclohexene-1 -yl)-2,4-pentadiene-1 -one]-L-proline and some of its salts were synthesized from β-ionylidenecyanoaeetic acid and tested for SHG.

Thesis (Ph. D. in Physics)--Vanderbilt University, Aug. 2008. / Title from title screen. Includes bibliographical references.

Thesis (Ph. D.)--University of Hong Kong, 2000. / Includes bibliographical references (leaves 280-300).