Download or read book Syntheses and Characterization of Mono and Dinuclear Complexes of Platinum Group Metals Bearing Benzene linked Bis pyrazolyl methane Ligands written by and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Mono and Dinuclear Half sandwich Platinum Group Metal Complexes Bearing Pyrazolyl pyrimidine Ligands Syntheses and Structural Studies written by and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Synthesis and Characterization of Mono and Dinuclear Platinum II Olefin Complexes Containing Pyrazole and Pyrazolato Ligands written by William Cullen Deese and published by . This book was released on 1982 with total page 276 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Mono and Dinuclear Complexes of Half sandwich Platinum Group Metals Ru Rh and Ir Bearing a Flexible Pyridyl thiazole Multidentate Donor Ligand written by and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Synthesis Luminescence and Host Guest Chemistry of Mono and Dinuclear Platinum ii Complexes of Pyridyl and Diphosphine Ligands written by Pui-Ling Tang and published by . This book was released on 2017-01-27 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: This dissertation, "Synthesis, Luminescence and Host-guest Chemistry of Mono- and Dinuclear Platinum(II) Complexes of Pyridyl and Diphosphine Ligands" by Pui-ling, Tang, 鄧佩玲, 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_b3124365 Subjects: Platinum Complex compounds Ligands Charge transfer
Download or read book Half Sandwich Platinum Group Metal Complexes Containing Tetradentate i N i donor Ligand Bearing Two Pyrazolyl pyridine Units Linked by an Aromatic Spacer written by and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Synthesis Luminescence and Host guest Chemistry of Mono and Dinuclear Platinum II Complexes of Pyridyl and Diphosphine Ligands written by Pui-ling Tang and published by . This book was released on 2002 with total page 646 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Syntheses Characterization and Photophysical Properties of Platinum ii and Gold i Complexes Containing Ortho And Meta Oligo phenyleneethynylene Ligands written by 朱明新 and published by Open Dissertation Press. This book was released on 2017-01-27 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: This dissertation, "Syntheses, Characterization and Photophysical Properties of Platinum(II) and Gold(I) Complexes Containing Ortho- and Meta-oligo(phenyleneethynylene) Ligands" by 朱明新, Mingxin, Zhu, 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 SYNTHESES, CHARACTERIZATION AND PHOTOPHYSICAL PROPERTIES OF PLATINUM(II) AND GOLD(I) COMPLEXES CONTAINING ORTHO- AND META- OLIGO(PHENYLENEETHYNYLENE) LIGANDS Submitted by Zhu Mingxin for the degree of Doctor of Philosophy at The University of Hong Kong in March 2008 Metal complexes containing oligo(phenyleneethynylene) (PE) are of great importance in photophysics and material science. The syntheses, characterizations and photophysical properties of the light-emitting platinum(II) and gold(I) complexes with flexible ortho- and meta-PE and 2,5-diphenyl-1,3,4-oxadiazole ligands were described. Several novel dinuclear terpyridyl platinum(II) complexes with ortho-PE ligands were synthesized and their crystal structures were determined. The t t 2+ t platinum(II) complexes [( Bu tpy)Pt-(ortho-PE)-Pt( Bu tpy)] ( Bu tpy = 4,4′,4″-tri- 3 3 3 tert-butyl-2,2′ 6′,2″-terpyridine) adopted a helical conformation in their crystal structures, and their phosphorescence recorded in acetonitrile/water mixtures shifted to lower energy with enhanced intensity when the water content increased. A hydrophobic folding process was suggested for the complexes with long ortho-PE(n) (n >= 3), and the red-shifted and enhanced phosphorescence was attributed to inter- and intra-molecular π-π interactions. The mononuclear terpyridine and C DEGREESN DEGREESN capped t + platinum(II) complexes [( Bu tpy)Pt-(ortho-PE)] and [(C DEGREESN DEGREESN)Pt-(ortho-PE)] (HC DEGREESN DEGREESN = 6-phenyl-2,2′-bipyridine) were studied for comparison. A series of mononuclear and dinuclear ortho- and meta-PE gold(I) complexes, [(PCy )Au-(ortho-PE)] (PCy = tricyclohexylphosphine), [(PCy )Au-(ortho-PE)- 3 3 3 Au(PCy)], [(PCy )Au-(meta-PE)] and [(PCy )Au-(meta-PE)-Au(PCy)] were 3 3 3 3 synthesized to examine the effect of ortho- and meta-conjugation. A ππ* emission of the PE ligands was switched on at room temperature by the attachment of [Au(PCy )] fragment due to the heavy atom effect. The delayed fluorescence from the ππ* excited states of the PE ligands was observed, and a triplet-triplet annihilation pathway was proposed. The difference in conjugation of para-, ortho- and meta-PE ligation was examined by comparison of the singlet and triplet emission energies of the gold(I) complexes. By extrapolating the plot of the emission energy against the PE chain length in the complex, the triplet emission energies of poly(ortho-PE) and poly(meta-PE) were estimated to be 530 and 470 nm respectively. These complexes together with the reported [Au(PCy )] complexes containing para-PE ligands, constitute a complete class of [Au(PCy )] supported phenyleneethynylene complexes. 2+ New ortho-PE ligands were used as flexible linkers for [Pt(PEt ) ] moieties 3 2 (PEt = triethylphosphine). Three neutral platinum(II) macrocycles with the maximum ring size of 60 atoms were synthesized and their crystal structures were determined, 31 revealing decreased nuclearity when the ortho-PE length increases. The P NMR spectra of [Pt(PEt ) {ortho-PE(5)}] with a rigid conformation at various temperatures 3 2 are consistent with the calculated spectrum of ABX spin system. A series of platinum(II)-bis(triethylphosphine) complexes containing 2,5- diphenyl-1,3,4-oxadiazole moiety were synthesized, and
Download or read book Synthesis Characterization and Redox Studies of Platinum and Palladium Complexes with Mer coordinating Ligands written by Seher Kuyuldar Tastan and published by . This book was released on 2009 with total page 206 pages. Available in PDF, EPUB and Kindle. Book excerpt: Synthetic, structural, spectroscopic, and redox studies of platinum(II) and palladium(II) compounds with mer-coordinating ligands have been undertaken in an effort to better understand the role of the metal and the ligands in controlling d^6/d^8 electron-transfer reactions. A series of Pd(pip2NCN)X (pip2NCNH=1,3-bis(piperdylmethyl)benzene) and [Pd(pip2NNN)X]X (X=Cl, Br, I) (pip2NNN=2,6- bis(piperdyl-methyl)pyridine) complexes are reported. Electronic spectra are consistent with stabilization of ligand-to-metal-charge-transfer states as the ancillary ligand is varied along the ClBr
Download or read book Synthesis and characterization of bismetalated platinum complexes containing benzothiophene functionalized ligands written by Asad Hashmi and published by . This book was released on 2016 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Synthesis and Investigation of Pyrazole containing Platinum Complexes for the Design of Macrocyclic Molecules and Potential Two electron Reagents written by Stuart Alan Willison and published by . This book was released on 2008 with total page 200 pages. Available in PDF, EPUB and Kindle. Book excerpt: A detailed study involving platinum(II) compounds with bis-2,6-pyrazolyl-phenyl type ligands have been undertaken in an effort to design a new architecture for building macrocyclic molecules with potentially coordinating tridentate ligands. Initial reports focused on platinum complexes with 2,6-bis-pyrazolyl-pyridine ligands. One complex, Pt(bpp)Ph +, exhibited an intense pink emission of the solid at 77 K, which is one of the first examples of a luminescent platinum compound with a bis-pyrazolyl-pyridine ligand. Herein we report the investigation of steric influence to promote C-H activation on the formation of monomeric and macrocyclic platinum(II) complexes, using methyl substituents on a series of anionic bis-pyrazolyl-phenyl ligands. Further studies of concentrated reaction mixtures at long reaction times result in exclusively trimeric products, whereas more dilute mixtures and shorter reaction times give only monomer products. Thus, careful control of the reaction conditions allows for selective activation of C-H bonds on the ligand giving isolated products of expected monomers and trimers, as well as surprising new dimeric products. In the course of our investigations of the monomeric platinum(II) products, we have discovered that four complexes react with dithiocarbamate accelerators most commonly used in latex processing, giving a colored response. Thus, the platinum complexes can be used as colorimetric indicators to detect allergenic dithiocarbamate compounds in latex products. In addition, we describe the synthesis and preliminary characterization of a potential two-electron reagent using a monomeric complex, Pt(4)Cl, and pip 2NNN, where 4 is 1,3-bis(3,5-dimethylpyrazolyl)benzene and (pip 2NNN) is 2,6-bis(piperidylmethyl)pyridine, to give Pt(4)(pip 2NNN) +.
Download or read book Synthesis and Characterization of Platinum II Complexes with Adamantantanamine Derivatives and Related Ligands written by Monique Doyon and published by . This book was released on 1991 with total page 356 pages. Available in PDF, EPUB and Kindle. Book excerpt: "New platinum(II) complexes of the type (Pt(A$ sp prime$)Cl$ sb3 rbrack sp-$, Pt(A)(A$ sp prime$)Cl$ sb2$ and Pt(A)(A$ sp prime$)I$ sb2$, where A = methylamine, ethylamine, cyclobutylamine and cyclopentylamine and A$ sp prime$ = 1-adamantanamine, 2-adamantanamine and 1-methyladamantanamine have been synthesized. The structure of (2-adamH) (Pt(EtNH$ sb2$)Cl$ sb3$) complex has been determined by X-ray diffraction." --
Download or read book Scorpionates The Coordination Chemistry Of Polypyrazolylborate Ligands written by Swiatoslaw Trofimenko and published by World Scientific. This book was released on 1999-08-16 with total page 294 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book deals with polypyrazolylborates (scorpionates), a class of ligands known since 1966, but becoming rapidly popular with inorganic, organometallic and coordination chemists since 1986, because of their versatility and user-friendliness. They can be readily modified sterically and electronically through appropriate substitution on the pyrazole ring and on boron, and have led to a number of firsts in coordination chemistry (first stable CuCO complex, first monomeric MgR complex, and many other such firsts). Their denticity can range from two to four, their “Bite” can be adjusted, and additional coordinating sites can be added to the pyrazolyl rings. Over 170 different scorpionate ligands are known today, and some are published for the first time in this book.The author, Swiatoslaw Trofimenko, discovered and developed this ligand system and has written several reviews on the subject. The book is intended as a reference work, placing at the researcher's command practically all of the over 1500 references on the subject up, and into 1999, organized both according to the ligand type and according to the metal or metalloid being coordinated. It acquaints the reader with the special features of this ligand system and permits an assessment of what has been done in a given sub-area, and of which areas remain relatively unexplored. It presents procedures for ligand synthesis, and also covers their use in catalysis and in the modelling of biologically active substances.
Download or read book Design Synthesis and Reactivity of Bimetallic Complexes of Dimethylplatinum II Containing Ditopic Ligands written by Matthew S. McCready and published by . This book was released on 2015 with total page 658 pages. Available in PDF, EPUB and Kindle. Book excerpt: This thesis describes a study of monometallic and bimetallic dimethylplatinum(II) complexes containing ditopic nitrogen donor ligands. This work details the design and synthesis of side-to-side and cofacial arranged ligands and their respective coordination chemistry. The study of the synthesis, characterization and reaction mechanisms of the various dimethylplatinum(II) complexes is outlined in detail with special emphasis focused on the reactivity of the complexes towards oxidative addition. The ditopic ligand 6-dppd, 1,4-di(2-pyridyl)-5,6,7,8,9,10- hexahydrocycloocta[d]pyridazine, was observed to coordinate only a single equivalent of a platinum(II) center. The inability to coordinate a second equivalent, even through an assisted bridging atom, is presumed to be due to a steric clash between the free pyridyl group and the cyclooctyl backbone. In attempts to make heterobimetallic complexes of 6-dppd, the complex [PtMe2(6-dppd)] was observed to react preferentially with mercuric halides by oxidative addition rather than coordination of the mercuric salt in the second coordination site giving complexes [PtXMe2(HgX)(6-dppd)] where X = Br, Cl, OAc. This indicates that the platinum center is actually a better nucleophile than the free pyridyl nitrogen atom. The oxidative addition of solvent dichloromethane was also observed showing the enhancedreactivity of [PtMe2(6-dppd)]. Finally, [PtMe2(6-dppd)] was treated with DCl at low temperature to give the deuteridoplatinum(IV) complex. The deuteridoplatinum(IV) complex reductively eliminates methane in solution and extensive H/D exchange occurs into the CH4 product at low temperature indicating very easy reversibility of the exchange between hydridomethylplatinum(IV) and methaneplatinum(II) complexes. The abstraction of a chloride ligand from [PtClMe(6-dppd)] led to the formation of a complex dimer structure endo, endo-[Pt2Me2(?2-?3-6-dppd)2][OTf]2. This process allowed for the formation of a bimetallic platinum(II) complex which retained the initial stereochemistry. The protonolysis of [PtMe2(6-dppd)] with one equivalent of HOTf led to the generation of methane gas and the concomitant formation of both endo, endo-[Pt2Me2(?2-?3-6-dppd)2][OTf]2 and exo, exo-[Pt2Me2(?2-?3-6-dppd)2][OTf]2. The structures of the exo isomeric clamshell dimers appeared much less sterically hindered in the solid state and were observed experimentally and computationally to be the thermodynamically preferred isomers. The mechanism, selectivity and reversibility of this isomerism process was explored in detail. The reactions of [PtMe2(6-dppd)] with alkyl bromides RCH2Br, which possess hydrogen bonding functionality, result in the formation of stable organoplatinum(IV) complexes capable of forming supramolecular structure via hydrogen bonding. Both intra and inter molecular hydrogen bonding is observed in the formation of supramolecular architectures which self-assemble in the solid state through additional?-stacking and weak secondary interactions. The new anthracene derived ditopic ligands, bpad = N1,N8-bis(pyridin-2- ylmethylene)anthracene-1,8-diamine and adpa = (N, N)-4,4'-(anthracene-1,8-diylbis(ethyne- 2,1-diyl))-bis(N-(pyridin-2-ylmethylene)aniline) were prepared, characterized and used to coordinate dimethylplatinum(II) centers giving cofacial bimetallic complexes of dimethylplatinum(II). [Pt2Me4(bpad)] was shown to degrade over time in solution through a proposed metalation event involving the anthracene backbone. The oxidative addition of a variety of substrates was performed using [Pt2Me4(adpa)] giving stable diplatinum(IV) complexes as characterized by 1H NMR spectroscopy. The new xanthene derived ditopic ligands, ppxda = 2,7-di-tert-butyl-9,9-dimethyl-N4,N5-bis(4-(pyridin-2- ylmethyleneamino)phenyl)-xanthene-4,5-dicarboxamide and pmxda = 2,7-di-tert-butyl-9,9- dimethyl-bis(pyridine-2-ylmethylene)-9H-xanthene-4,5-diamine were prepared characterized and used to ligate two equivalents of a dimethylplatinum(II) center. Diplatinum complexes of both ligands were shown to easily undergo oxidative addition to give the corresponding diplatinum(IV) complexes which adopt the anti orientation. The syn alignment of metal centers was accessible through the abstraction of halides ligands and incorporation of bridging groups as is the case for the pyrazine bridged bimetallic platinum complex [Pt2Me6(C4H4N2)(pmxda)][OSO2CF3]2.
Download or read book Synthesis and Reactivity of PtII Complexes with Secondary Sphere N H Moieties written by Braden A. Zahora and published by . This book was released on 2019 with total page 194 pages. Available in PDF, EPUB and Kindle. Book excerpt: Direct transformations of abundant hydrocarbons into higher valued products would circumvent energy intensive processes, reforming the chemical industry. Late transition metals, particularly platinum, are known to selectively convert alkanes into functionalized products. However, a practical method with an economically viable oxidant has yet to be discovered. New methods for alkane activation may yield further advances towards this goal. This dissertation focuses on how platinum methyl complexes with ligand-based protons can form methane, the microscopic reverse of methane activation. Chapter 1 provides an introduction on the need to develop new methods to functionalize hydrocarbons. Furthermore, a survey of the literature with respect to how late metal complexes can undergo productive reactivity with substrates which are deemed necessary for practical alkane partial oxidation is presented. Chapter 2 focuses on the synthesis and reactivity of 5-(6-methyl-2-pyridyl)-3-tert-butylpyrazolate (NN[superscript]Me) and 2-(5-tert-butylpyrazol-3-yl)-6 (diethylaminomethyl)pyridine (NNN[superscript]Et) ligated Pt[superscript]II complexes. Once formed, conditions necessary for methane formation were found and it was determined that the ligand-based N-H was not involved in methane formation. Chapter 3 explores synthesis and reactivity of 5-tert-butyl-1,3-bis(pyrazol-3-yl)pyridine (NNN) and 5-tert-butyl-1,3-bis(pyrazol-3-yl)benzene (NCN) ligated Pt[superscript]II-alkyl complexes with electrophilic reagents. It was found that tridentate ligated pyrazolate Pt[superscript]II-R systems can undergo protonation at the ligand if there is a weak pyridine trans donor (vs strong phenyl trans donor) to the Pt[superscript]II-R moiety. However, reactivity with methyl iodide occurred at the metal first, with further ligand methylation spectroscopically observed for the NNN ligated Pt-CH3 complex. Chapter 4 discusses the synthesis and characterization of bis(phosphino)amine ligated Pt[superscript]II complexes, which contained a ligand-based N-H. Taking advantage of unfavorable steric congestion of bulky Ph groups on the ligand, methane formation was observed from thermolysis reactions of a bis(phosphino)amine ligated Pt(CH3)2. Although additional characterization of the resulting metal-containing product is required, it appears that methane was formed through cooperation of the ligand-based N-H moiety and the Pt-CH3 ligand.
Download or read book Design and Synthesis of Luminescent Mono And Dinuclear Platinum ii Alkynyl Terpyridine Complexes written by Hoi-Yiu Chan and published by Open Dissertation Press. This book was released on 2017-01-27 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: This dissertation, "Design and Synthesis of Luminescent Mono- and Dinuclear Platinum(II) Alkynyl Terpyridine Complexes: From Photophysics to Aggregation and Self-assembly" by Hoi-yiu, Chan, 陳凱耀, 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 AND SYNTHESIS OF LUMINESCENT MONO- AND DINUCLEAR PLATINUM(II) ALKYNYL TERPYRIDINE COMPLEXES - FROM PHOTOPHYSICS TO AGGREGATION AND SELF-ASSEMBLY submitted by CHAN Hoi Yiu for the degree of Doctor of Philosophy at The University of Hong Kong in August 2006 A series of mononuclear alkynylplatinum(II) terpyridyl complexes, [Pt(trpy)({C{ C} C H )]PF, [Pt(trpy)({C{ C} C H CF -4)]PF, n 6 5 6 n 6 4 3 6 [Pt(trpy)({C{ C} C H CH -4)]PF, and [Pt( Bu trpy)(C{ C C{ C C H )]PF (n = n 6 4 3 6 3 6 5 6 2, 3), have been synthesized. The X-ray crystal structures of the two forms of [Pt(trpy)(C{ C C{ C C H )]PF, [Pt(trpy)(C{ C C{ C C{ C C H CH -4)]PF and 6 5 6 6 4 3 6 [Pt( Bu trpy)(C{ C C{ C C H )]PF have been determined. Dinuclear and 3 6 5 6 trinuclear alkynylplatinum(II) terpyridyl complexes, [1,4- {Pt(trpy)C{ C} C H ](OTf), [1,4-{Pt( Bu trpy)C{ C} C H ](OTf), [2,5- 2 6 4 2 3 2 6 4 2 {Pt(trpy)C{ C} C H S](OTf), [2,5-{Pt( Bu trpy)C{ C} C H S](OTf) and [1,3,5- 2 4 2 2 3 2 4 2 2 {Pt( Bu trpy)C{ C} C H ](OTf) have been successfully synthesized. The X-ray 3 3 6 3 3t crystal structure of [1,4-{Pt( Bu trpy)C{ C} C H ](OTf) has also been 3 2 6 4 2 determined. The luminescence properties of these complexes have been studied and their lowest-lying excited states in fluid solution and in the glass state were tentatively assigned as admixture of MLCT [dS (Pt)ĺ S *(trpy)] and LLCT [S (C{ C)ĺ S *(trpy)] origin, whereas the low-energy emissions in the solid state were attributed to triplet metal metal-to-ligand charge transfer ( MMLCT) phosphorescence, resulting from significant Pt---Pt interactions in the solid state. Besides, a series of luminescent platinum(II) terpyridyl alkynyl complexes with different counter anions, [Pt(trpy)(C{ C C{ C H)]X (X = OTf, PF, ClO, 6 4 BF, BPh ), [Pt(trpy)(C{ C C H )]X (X = OTf, PF, ClO, BF ) and 4 4 6 5 6 4 4 complexes with various substituents on the alkynyl and terpyridyl ligands, [Pt(trpy)(C{ CC H OCH-4)]OTf, [Pt(4'-CH O trpy)(C{ C C H )]OTf, 6 4 3 3 6 5 [Pt( Bu trpy)(C{ C C{ CH)]OTf, [Pt(trpy)(C{ CC H {CH NMe }-4)](OTf), 3 6 4 2 3 2 [Pt(trpy)(C{ C C{ C CH NMe )](OTf) and [Pt(trpy)(C{ C C{ C CH OH)]OTf 2 3 2 2 have been synthesized and their photophysical properties have been stuided. The X-ray crystal structure of [Pt(trpy)(C{ C C H )]ClO and 6 5 4 [Pt( Bu trpy)(C{ C C{ C H)]OTf have been determined. The solid-state absorption and emission spectra showed low-energy bands, which were assigned as derived from MMLCT origin. Solvent-induced aggregation studies of these complexes in solution showed that the color of the aggregates could be very different for different counter-ions, indicating that counter-ions played an important role in governing the degree of aggregation and the extent of interactions within these aggregates. Addition of various anions to solutions of [Pt(trpy)(C{ C C{ C H)]X (X = OTf, PF ) produced anion-induced color 6changes upon solvent-induced aggregation, showing that these complexes might serve as potential colorimetric anion probes. The effect of temperature on the aggregation properties of the complexes has also been explored. New low-energy absorption and emission bands were found upon a reduction of temperature, attributable to the formation o
Download or read book Synthesis and Characterization of Binuclear and Transition Metal Complexes Incorporating the Tridentate Chelating Ligand Dimethyl N N dimethylethanolamino 1 pyrazolyl gallate written by and published by . This book was released on 1977 with total page 66 pages. Available in PDF, EPUB and Kindle. Book excerpt:
