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| Author | : Tiffany Anne Grant |
| Publisher | : |
| Total Pages | : 262 |
| Release | : 1998 |
| Genre | : |
| ISBN | : |
| Author | : Phuong (Lucy) Minh Cam Luong |
| Publisher | : |
| Total Pages | : 0 |
| Release | : 2020 |
| Genre | : |
| ISBN | : |
The research presented in this dissertation focuses on the synthesis, crystallization, and characterization of various gold(I) complexes. With every gold(I) crystal, intensive studies were conducted to uncover any luminescence, polymorphism, and/or response to environmental stimuli such as temperature, vapor, and pressure. All doctoral research performed in the Balch lab, including collaborations with other members as well as outside research groups, is not fully presented in this dissertation. A list of publications can be found at the end. Chapter 1 explores the role of anions and mixture of anions in crystals of bis(cyclohexylioscyanide) gold(I) cations, [(C6H11NC)2Au]+. A new crystal was synthesized and characterized with the (SbF6)− noncoordinating anion. The crystal displayed no known polymorphism unlike its previously synthesized (PF6)− and (AsF6)− analogues. However, by mixing combinations of anions and ratios of anions, an isostructural set of crystals were produced. Not only were thermochromic trends observed for mixed anion crystals with known thermochromic species but unexpected thermochromic properties appeared in mixed anion crystals that contained species with no thermochromism. In Chapter 2, the vapochromic and vapoluminescent properties of both [(C6H11NC)2Au](PF6) and [(C6H11NC)2Au](AsF6) were further investigated to uncover the first observed single-crystal-to-single-crystal phase transition, verified by single crystal X-ray diffraction, of both species. A rare case of a two-polymorph single crystal of each species was achieved as well. With no vapor molecules incorporated in these crystals, the mechanism of conversion was further examined at the macroscopic, microscopic, and atomic level to understand how these solvent-free crystals transform from solvent vapor exposure. Chapter 3 focuses on methods to isolate [(C6H11NC)2Au]+ to form non-luminescent crystals, which was achieved through bulky noncoordinating anions and solvent molecules. Newly synthesized [(C6H11NC)2Au](BArF24) was crystallized but showed no further interesting properties other than purposely isolating aurophilic interactions. However, the first solvates of these [(C6H11NC)2Au]+ series, C6H6·[(C6H11NC)2Au](AsF6) and C6H6·[(C6H11NC)2Au](SbF6), were crystallized that displayed a unique turning on of luminescence when left to dry that matched their solvent-free forms, as verified by powder X-ray diffraction, infrared spectroscopy, and fluorescence spectroscopy. Differing from the other studies, Chapter 4 examines the structure and luminescence of three-coordinate 2,2'-bipyridine gold(I) tertiary phosphine crystals. Separate isomorphic series of [(Ph3P)Au(bipy)]XF6 and [(Et3P)Au(bipy)]XF6 (where X = P, As, or Sb) along with binuclear [[mu]2-bipy(AuPPh3)2](PF6)2 were crystallized and showed no luminescence, which is unlike that of known strongly luminescent gold(I) phosphines. However, the three-coordinate [(Ph3P)Au(bipy)]XF6 and [(Et3P)Au(bipy)]XF6 complexes all displayed significantly unsymmetrical coordination of the gold(I) to the two nitrogen atoms in the 2,2'-bipyridine ligand. These large unsymmetrical distances were further investigated.
| Author | : Darkus Elizabeth Jenkins |
| Publisher | : |
| Total Pages | : 256 |
| Release | : 2012 |
| Genre | : Acetonitrile |
| ISBN | : |
Searches for methods of volatile organic compound sensor devices by the examination of photoluminescence and photoluminescent materials such as metal complexes. Shows the synthesis and structural characterization of the bridging ligand, 1-methylbenzimidazole diphenylphosphine. Examines the coordination mode of this ligand to gold and silver metals. Observes the stucture of the mononuclear gold complex, a gold dimer, and a silver dimer in non-polymeric form with notable differences around the metal center. Describes the electronic properties of the ligand and metal complexes. Explores the sensitivity of the dimer gold complex to acetonitrile.
| Author | : Amanda N. Sulicz |
| Publisher | : |
| Total Pages | : 264 |
| Release | : 2017 |
| Genre | : Complex compounds |
| ISBN | : |
The chemistry of cyclometalated gold(III) has been relatively slow to emerge, but recent advances in catalyst and material design have driven a renewed interest. Reported here are synthetic, structural, and optical studies of cyclometalated gold(III) aryl complexes. These new complexes show ligand-centered luminescence that is perturbed by the heavy-atom effect of gold. Traditionally, metal-carbon bond formation relied on organometallic complexes of electropositive elements, including lithium and magnesium. The easily reducible nature of gold(III) often interferes with these conventional reagents, thus resulting in the use of toxic metals like mercury or thallium. Reported here is the use of palladium-catalyzed Suzuki-Miyaura cross-coupling for the attachment of aryl ligands to cyclometalated gold(III) chloride complexes. The resulting di- and mono-arylated species were luminescent. Several complexes have been crystallographically characterized. Luminescent derivatives of a previously published gold(III) chloro precursor, initially reported for catalytic purposes, were prepared through boron transmetalation reactions. Complexes bearing both aryl and cyanide ligands were synthesized. These luminescent materials are diamagnetic and were be characterized by multinuclear NMR, absorption and emission spectroscopies (including time-resolved emission), and by X-ray diffraction crystallography. The synthesized gold(I) complexes were designed to display reverse saturable absorption and be a two photon acceptor. The BTF (BTF = 2-(9,9’-diethyl-9H-fluoren-2-yl)-benzothiazole) ligand was chosen as it has been previously demonstrated to have favorable photophysical effects on platinum(II) and ruthenium(II) complexes for applications in photodynamic therapy and optical power limiting (OPL). Gold(I) complexes with the BTF ligand are sought for potential OPL applications. Synthesized complexes are luminescent and were characterized by multinuclear NMR, absorption and emission spectroscopies, photoluminescent quantum yields, time-resolved emission. Two complexes were crystallographically characterized.
| Author | : Sung-Kong Yip |
| Publisher | : Open Dissertation Press |
| Total Pages | : |
| Release | : 2017-01-26 |
| Genre | : |
| ISBN | : 9781361235584 |
This dissertation, "Design, Synthesis, Characterization and Luminescence Properties of Alkynylgold(I) Complexes: Strategies Towards Supramolecular Architectures and Host Guest Chemistry" by Sung-kong, Yip, 葉崇江, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. Abstract: Abstract of thesis entitled DESIGN, SYNTHESIS, CHARACTERIZATION AND LUMINESCENCE PROPERTIES OF ALKYNYLGOLD(I) COMPLEXES STRATEGIES TOWARDS SUPRAMOLECULAR ARCHITECTURES AND HOST GUEST CHEMISTRY Submitted by YIP Sung Kong for the degree of Doctor of Philosophy at The University of Hong Kong in July 2005 A series of luminescent dialkynylaurate(I) complexes, [X][Au(C CR) ] [X = Bu N, R = C H OMe-p, C H OHex-p, C H Oct-p, C H Cl-p, C H CF -p, 1-naphthyl 4 6 4 6 4 6 4 6 4 6 4 3 (Np), 9-anthracenyl (An), 1-pyrenyl (Pyr); X = PPN, R = Pyr] have been synthesized. The X-ray crystal structures of [BuN][Au(CCCHOMe-p)] and 4 64 2 [BuN][Au(CCCHCF-p)] showed the presence of intermolecular hydrogen 4 64 3 2 bonds with bonding distances of ca. 2.599 - 2.620 A. The related pentanuclear gold(I)-copper(I) and -silver(I) mixed-metal alkynyl complexes, [BuN][AuM(CCCH-R-p) ] [M = Cu, R = OMe, OBu, OHex, Et; M = Ag, R = Et, 4 32 64 6 OHex] have been synthesized. The emission origin was tentatively assigned as derived from triplet states of metalloligand-to-metal cluster core charge transfer [Au(C CR) M Au ] (M = Cu, Ag) origin, probably mixed with some metal- 2 2 3 perturbed intraligand *(C C) character. Through the utilization of alkynylcalix[4]crown as ligands, dinuclear gold(I) 1 2 3 alkynylcalix[4]crown-5 complexes, [(R P)Au] L [R = Tol-o, L = L; R = Ph, L = L, L ], 3 2 4 5 6 1 tetranuclear gold(I) alkynylcalix[4]crown assemblies, [Au (L') ] [L' = L, L, L, L ] and 4 2 a mixed-metal gold(I)-copper(I) alkynylcalix[4]crown complex, [Au Cu (L ) ] have 2 2 2 been synthesized. The X-ray crystal structures of all the dinuclear gold(I) complexes, 4 1 4 [Au (L') ] [L' = L, L ] and [Au Cu (L ) ] have been determined. The X-ray crystal 4 2 2 2 2 structures of [Au(L')] showed that two of the gold(I) centers were each 4 2 -coordinated to two alkynyl units, while the other two were each -coordinated by 2 2 the two alkynyl units in an unusual planar, -coordination mode, which was the first of its kind for gold(I) complexes. The Au Au distances between adjacent gold atoms were in the range of 3.1164(11) 3.2118(10) A, indicative of the presence of significant Au Au interactions. The emissive origin of [Au (L') ] was assigned as 4 2 derived from a triplet state of a metal cluster-centered ds/dp character, probably with some mixing of a metal-perturbed intraligand character, while the emission of [Au Cu (L ) ] was assigned to have similar character, but with modification by 2 2 2 Au Cu interactions. The binding properties of the dinuclear gold(I) complexes toward alkali metal ions have been studied. Dinuclear gold(I) complexes, [{Ph PN(R)PPh }Au (C CR') ] [R = Pr, R' = Ph, 2 2 2 2 C H OMe-p, C H Me-p, C H Cl-p; R = C H OMe-p, R' = Ph], have been synthesized 6 4 6 4 6 4 6 4 by deploymerization of alkynylgold polymers using bis(diphenylphosphino)amines as ligands. The X-ray crystal structures of [{PhPN(Pr)PPh}Au(C CPh)] and 2 2 2 2 [{PhPN(Pr)PPh}Au(C CCHOMe-p)]] revealed the presence of short 2 2 2 6 4 2 intramolecular Au Au contacts with the Au Au distances of 2.8404(8) and 3.0708(7) A, respectively. The photophysical properties of the complexes have been studied and their emission orig
| Author | : Lauren Christine Eiter |
| Publisher | : |
| Total Pages | : 226 |
| Release | : 2007 |
| Genre | : Cancer |
| ISBN | : |
| Author | : 張啓亮 |
| Publisher | : |
| Total Pages | : |
| Release | : 2017-01-28 |
| Genre | : |
| ISBN | : 9781374793071 |
This dissertation, "Syntheses and Luminescence Studies of Di- and Polynuclear Gold(1) and Copper(1) Complexes, Design Strategies Towards Metalloreceptors and Mixed-metal Complexes" by 張啓亮, Kai-leung, Cheung, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. DOI: 10.5353/th_b3124299 Subjects: Gold - Synthesis Copper compounds - Synthesis Complex compounds - Spectra Photochemistry
| Author | : Kwok-Ming Lee |
| Publisher | : |
| Total Pages | : |
| Release | : 2017-01-26 |
| Genre | : |
| ISBN | : 9781361273166 |
This dissertation, "Synthesis, Characterization and Photophysical Properties of Chalcogenido, Phosphinidene and Alkynyl Complexes of Gold (I) and Its Congener and Their Supramolecular Assembly Arising From Metal--metal Interactions" by Kwok-ming, Lee, 李國明, was obtained from The University of Hong Kong (Pokfulam, Hong Kong) and is being sold pursuant to Creative Commons: Attribution 3.0 Hong Kong License. The content of this dissertation has not been altered in any way. We have altered the formatting in order to facilitate the ease of printing and reading of the dissertation. All rights not granted by the above license are retained by the author. DOI: 10.5353/th_b4598342 Subjects: Gold compounds - Synthesis Complex compounds - Synthesis Photochemistry Supramolecular chemistry
| Author | : D. Max Roundhill |
| Publisher | : Springer Science & Business Media |
| Total Pages | : 422 |
| Release | : 2013-03-09 |
| Genre | : Science |
| ISBN | : 1475761015 |
This book is intended to offer the reader a snapshot of the field of optoelectronic materials from the viewpoint of inorganic chemists. The field of inorganic chemistry is transforming from one focused on the synthesis of compounds having interesting coordination numbers, structures, and stereochemistries, to one focused on preparing compounds that have potentially useful practical applica tions. Two such applications are in the area of optics and electronics. These are fields where the use of inorganic materials has a long history. As the field of microelectronics develops the demands on the performance of such materials increases, and it becomes necessary to discover compounds that will meet these demands. The field of optoelectronics represents a merging of the two disciplines. Its emergence is a natural one because many of the applications involve both of these properties, and also because the electronic structure of a metal compound that confers novel optical properties is often one that also influences its electron transfer and conductivity characteristics. Two of the more important growth areas that have led to these developments are communications and medicine. Within the communications field there is the microelectronics that is involved in information storage and transmittal, some of which will be transferred into the optical regime. Within the medical field there are chemical probes that transmit analytical information from an in vivo environment. This information needs to be readily accessible from an external site, and then quickly converted into images or data that yield accurate and inexpensive diagnoses.
| Author | : Chui-Ling Chan |
| Publisher | : |
| Total Pages | : |
| Release | : 2017-01-26 |
| Genre | : |
| ISBN | : 9781361193648 |
