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LUMINESCENT PALLADIUM(II) & PL

LUMINESCENT PALLADIUM(II) & PL PDF Author: Pui-Keong Chow
Publisher: Open Dissertation Press
ISBN: 9781361005378
Category : Science
Languages : en
Pages : 502

Book Description
This dissertation, "Luminescent Palladium(II) and Platinum(II) Complexes With Tridentate Monoanionic and Tetradentate Dianionic Cyclometallated Ligands: Structures, Photophysical Properties and Material Application" by Pui-keong, Chow, 周沛強, 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: Four structural isomers of platinum(II) complexes with C-deprotonated R-C DEGREESN DEGREESN-R' cyclometallated ligands (R-C DEGREESN DEGREESN-R' = -extended 6-aryl-2,2'-bipyridine derivatives containing 2-naphthyl, 3-isoquinolinyl, 1-isoquinolinyl or 2-quinolinyl moieties) have been synthesized with their photophysical properties investigated. The one bearing a 3-isoquinolinyl moiety shows the highest emission quantum yield among the four and hence has been extensively modified to give a series of complexes with different ancillary ligands (chloride, iodide, phenoxide, or acetylide). Most of these complexes show vibronic emission (max = 515-644 nm) with high emission quantum yield (up to unity) in degassed CH2Cl2; one of them has been used for OLED fabrication and shows a maximum EQE of 8.15 % with current efficiency of 25 cd A-1. The photocatalytic properties of these derivative complexes for oxidative tertiary amine functionalization have also been examined. Several highly robust and emissive platinum(II) complexes supported by two types of tetradentate O DEGREESN DEGREESC DEGREESN ligand systems (Φem up to 0.99; Td up to 520 ℃) have been synthesized and show different emission energies (λmax = 482-561 nm). Most of them exhibit excimeric emission in solution state at room temperature which are dependent on the modifications on the tetradentate O DEGREESN DEGREESC DEGREESN ligands. DFT/TDDFT calculations reveal that the metal complex showing the most intense excimeric emission possesses an excimeric excited state with a localized structure, which is unusual for these classes of platinum(II) complexes. Based on this finding, WOLED (ηL(max) = 71.0 cd/A, ηp(max) = 55.8 lm/W, ηExt = 16.5 %, CIE = 0.33, 0.42, CRI = 77) and WPLED (ηL(max) = 17.0 cd/A, ηp(max) = 9.1 lm/W, ηExt = 9.7 %, CIE = 0.43, 0.45, CRI = 78) based on this complex have been fabricated with high efficiency achieved. Palladium(II) complexes containing C-deprotonated R-C DEGREESN DEGREESN-R' cyclometallated and pentafluorophenylacetylide ligands exhibit phosphorescence in both solid state and fluid solutions at room temperature with some of them exhibiting aggregation-induced emission (AIE). These complexes have been applied as photosensitizers in light-induced oxidative functionalization of secondary and tertiary benzylic amines as well as in light-induced hydrogen production, with a maximum of 175 turnovers for hydrogen produced. Palladium(II) complexes containing two types of tetradentate dianionic O DEGREESN DEGREESC DEGREESN ligand systems (Systems 1 and 2) have been prepared and show constrasting photophyical properties. A full scale time-resolved spectroscopic analysis has been done on some of these complexes and a platinum(II) analogue. These complexes are found to have similar excited state decay pathway( 〖S_1〗 DEGREESi→〖S_1〗 DEGREESf→T) with ΦISC of about unity. The emission efficiency of System 2 complexes is superior to that of System 1 complexes, which is ascribed to the suppression of excited state distortion on the basis of the results of DFT calculations. A lower radiative decay rate of System 2 palladium(II) complexes relative to the platinum(II) analogue has been found, which could be due to their lower spin-orbit coupling constant. One of the palladium(II) complexes ha

LUMINESCENT PALLADIUM(II) & PL

LUMINESCENT PALLADIUM(II) & PL PDF Author: Pui-Keong Chow
Publisher: Open Dissertation Press
ISBN: 9781361005378
Category : Science
Languages : en
Pages : 502

Book Description
This dissertation, "Luminescent Palladium(II) and Platinum(II) Complexes With Tridentate Monoanionic and Tetradentate Dianionic Cyclometallated Ligands: Structures, Photophysical Properties and Material Application" by Pui-keong, Chow, 周沛強, 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: Four structural isomers of platinum(II) complexes with C-deprotonated R-C DEGREESN DEGREESN-R' cyclometallated ligands (R-C DEGREESN DEGREESN-R' = -extended 6-aryl-2,2'-bipyridine derivatives containing 2-naphthyl, 3-isoquinolinyl, 1-isoquinolinyl or 2-quinolinyl moieties) have been synthesized with their photophysical properties investigated. The one bearing a 3-isoquinolinyl moiety shows the highest emission quantum yield among the four and hence has been extensively modified to give a series of complexes with different ancillary ligands (chloride, iodide, phenoxide, or acetylide). Most of these complexes show vibronic emission (max = 515-644 nm) with high emission quantum yield (up to unity) in degassed CH2Cl2; one of them has been used for OLED fabrication and shows a maximum EQE of 8.15 % with current efficiency of 25 cd A-1. The photocatalytic properties of these derivative complexes for oxidative tertiary amine functionalization have also been examined. Several highly robust and emissive platinum(II) complexes supported by two types of tetradentate O DEGREESN DEGREESC DEGREESN ligand systems (Φem up to 0.99; Td up to 520 ℃) have been synthesized and show different emission energies (λmax = 482-561 nm). Most of them exhibit excimeric emission in solution state at room temperature which are dependent on the modifications on the tetradentate O DEGREESN DEGREESC DEGREESN ligands. DFT/TDDFT calculations reveal that the metal complex showing the most intense excimeric emission possesses an excimeric excited state with a localized structure, which is unusual for these classes of platinum(II) complexes. Based on this finding, WOLED (ηL(max) = 71.0 cd/A, ηp(max) = 55.8 lm/W, ηExt = 16.5 %, CIE = 0.33, 0.42, CRI = 77) and WPLED (ηL(max) = 17.0 cd/A, ηp(max) = 9.1 lm/W, ηExt = 9.7 %, CIE = 0.43, 0.45, CRI = 78) based on this complex have been fabricated with high efficiency achieved. Palladium(II) complexes containing C-deprotonated R-C DEGREESN DEGREESN-R' cyclometallated and pentafluorophenylacetylide ligands exhibit phosphorescence in both solid state and fluid solutions at room temperature with some of them exhibiting aggregation-induced emission (AIE). These complexes have been applied as photosensitizers in light-induced oxidative functionalization of secondary and tertiary benzylic amines as well as in light-induced hydrogen production, with a maximum of 175 turnovers for hydrogen produced. Palladium(II) complexes containing two types of tetradentate dianionic O DEGREESN DEGREESC DEGREESN ligand systems (Systems 1 and 2) have been prepared and show constrasting photophyical properties. A full scale time-resolved spectroscopic analysis has been done on some of these complexes and a platinum(II) analogue. These complexes are found to have similar excited state decay pathway( 〖S_1〗 DEGREESi→〖S_1〗 DEGREESf→T) with ΦISC of about unity. The emission efficiency of System 2 complexes is superior to that of System 1 complexes, which is ascribed to the suppression of excited state distortion on the basis of the results of DFT calculations. A lower radiative decay rate of System 2 palladium(II) complexes relative to the platinum(II) analogue has been found, which could be due to their lower spin-orbit coupling constant. One of the palladium(II) complexes ha

Luminescent Platinum(II), Palladium(II) and Gold(III) Complexes Containing Isocyanide, Alkynyl and N-heterocyclic Carbene Ligands

Luminescent Platinum(II), Palladium(II) and Gold(III) Complexes Containing Isocyanide, Alkynyl and N-heterocyclic Carbene Ligands PDF Author: 孔繁峰
Publisher:
ISBN:
Category : Organogold compounds
Languages : en
Pages : 580

Book Description


Luminescent Platinum(ii), Palladium(ii) and Gold(iii) Complexes Containing Isocyanide, Alkynyl and N-Heterocyclic Carbene Ligands

Luminescent Platinum(ii), Palladium(ii) and Gold(iii) Complexes Containing Isocyanide, Alkynyl and N-Heterocyclic Carbene Ligands PDF Author: Faan-Fung Hung
Publisher: Open Dissertation Press
ISBN: 9781361385418
Category :
Languages : en
Pages :

Book Description
This dissertation, "Luminescent Platinum(II), Palladium(II) and Gold(III) Complexes Containing Isocyanide, Alkynyl and N-heterocyclic Carbene Ligands: Synthesis, Photophysical Properties and Material Applications" by Faan-fung, Hung, 孔繁峰, 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: Several cyclometalated Pt(II) isocyanide complexes containing C-deprotonated C DEGREESN DEGREESC ligands (C DEGREESN DEGREESC = 2,6-diphenylpyridine derivatives) were synthesized. These complexes display orange-red emissions with max at 582-619 nm and quantum yields of up to 26% in CH2Cl2 at room temperature. The incorporation of carbazole/fluorene/thiophene unit(s) to C DEGREESN DEGREESC ligands leads to minimized structural distortion of complexes in their excited states and thereby suppresses non-radiative decay pathways. The high thermal stability (Td >300 C) renders these complexes good candidates as phosphorescent dopants in organic light-emitting diodes (OLEDs). Red-emitting OLEDs with CIE coordinates of (0.650.01, 0.350.01) were fabricated by vacuum deposition, showing a maximum external efficiency of 12%. In addition, well-defined nano/microstructures were obtained from self-assembly of these complexes driven by π∙∙∙π, C-H∙∙∙π and C-H∙∙∙H-C interactions as observed in the crystal structures. Two series of organopalladium(II) alkynyl complexes containing a terpy (terpy = 2,2':6',2''-terpyridine) or C DEGREESN DEGREESC pincer carbene ligand (C DEGREESN DEGREESC = 2,6-bis(1-butylimidazol-2-ylidenyl)pyridine) were prepared. These complexes are non-emissive in solution at room temperature except that the one containing both C DEGREESN DEGREESC and pyrenylacetylide ligands shows phosphorescence (Φ = 0.3%) originating from intraligand state of the acetylide ligand. This could be attributed to the strong -donating N-heterocyclic carbene (NHC) in the pincer ligand that strongly destabilizes d-d state, the population of which provides an efficient non-radiative decay channel. To make comparison between Pd(II) and Pt(II) complexes with the two ligand systems, Pt(II) C DEGREESN DEGREESC alkynyl complexes were also prepared. They are emissive in solution and some display excimer emissions at high concentration (〖10〗 DEGREES(-4)-〖10〗 DEGREES(-3) mol 〖10dm〗 DEGREES(-3)). The X-ray crystal structures of [Pd(L)(CCPh)](〖PF〗_6) (L = terpy and C DEGREESN DEGREESC) revealed one-dimensional chain stacking of complex cations with alternating Pd(II)∙∙∙Pd(II) contacts of about 3.29-3.35 A and π-π interactions of about 3.4 A . Well-defined submicron/nanostructures were obtained from self-assembly of Pd(II) and Pt(II) alkynyl complexes driven by π-π interactions between aromatic moieties and/or metal∙∙∙metal interactions. DFT calculations on the optimized structures of [M(L)(CCPh)]+ (M = Pd(II) and Pt(II)) revealed the existence of metal∙∙∙metal closed-shell interactions. In addition, the complex containing the C DEGREESN DEGREESC ligand exhibits slightly enhanced metal∙∙∙metal interactions and larger "bonding" energy upon dimerization. Furthermore, spin-orbit coupling between singlet and triplet excited states is more effective which promotes rapid intersystem crossing. A new class of cyclometalated Au(III) complexes containing C-deprotonated C DEGREESN ligands (C DEGREESN = 2-phenylpyridine and its derivatives) and cis-chelating bis-NHC ligands was synthesized. These are the first examples of Au(III) complexes supported by cis-chelating bis-NHC ligands. They display emissions in solution under degassed condition at room temperature with &

Luminescent Palladium(II) and Platinum(II) Complexes with Tridentate Monoanionic and Tetradentate Dianionic Cyclometallated Ligands

Luminescent Palladium(II) and Platinum(II) Complexes with Tridentate Monoanionic and Tetradentate Dianionic Cyclometallated Ligands PDF Author: Pui-keong Chow
Publisher:
ISBN:
Category : Metal complexes
Languages : en
Pages : 480

Book Description


Luminescent Palladium(II) and Platinum(II) Complexes with Tridentate Monoanionic and Tetradentate Dianionic Cyclometallated Ligands

Luminescent Palladium(II) and Platinum(II) Complexes with Tridentate Monoanionic and Tetradentate Dianionic Cyclometallated Ligands PDF Author: Pui-keong Chow
Publisher:
ISBN:
Category : Metal complexes
Languages : en
Pages : 0

Book Description


Reactivity in Confined Spaces

Reactivity in Confined Spaces PDF Author: Gareth O. Lloyd
Publisher: Royal Society of Chemistry
ISBN: 1788017765
Category : Science
Languages : en
Pages : 491

Book Description
This title combines classical host: guest chemistry with catalysis, reactivity and modern supramolecular chemistry

Photochemistry and Photophysics of Coordination Compounds

Photochemistry and Photophysics of Coordination Compounds PDF Author: Hartmut Yersin
Publisher: Springer Science & Business Media
ISBN: 3642726666
Category : Science
Languages : en
Pages : 334

Book Description
Proceedings of the Seventh International Symposium on the Photochemistry and Photophysics of Coordination Compounds Elmau/FRG, March 29-April 2, 1987

Upconversion Nanophosphors

Upconversion Nanophosphors PDF Author: Sabu Thomas
Publisher: Elsevier
ISBN: 0128228431
Category : Technology & Engineering
Languages : en
Pages : 426

Book Description
Upconversion Nanophosphors provides detailed information about various lanthanide-based upconversion nanoparticles and their application in different fields. It will also help solve fundamental and applied problems of inorganic phosphor materials showing upconversion behavior, as well as generate innovative ideas related to the application of inorganic phosphor materials. This book will prove to be an invaluable reference work for scientists, engineers, industrial experts, and masters and PhD students working in the field of upconversion and materials science. Covers the synthesis and characterization of upconversion nanophosphors and their applications Highlights which classes of upconversion materials are suitable for a specific application Explores processes to engineer upconversion nanoparticles for state-of-the-art technologies, including upconversion labelling and counterfeiting, highly sensitive and selective biosensing, and upconversion-activated drug delivery

Metallomesogens

Metallomesogens PDF Author: Jose Luis Serrano
Publisher: John Wiley & Sons
ISBN: 3527615083
Category : Technology & Engineering
Languages : en
Pages : 517

Book Description
Research on metal-containing liquid crystals is a rapidly expanding, multidisciplinary field with new materials continually being synthesized and novel applications being developed. 'Metallomesogens' is the first comprehensive survey of the field, introducing the reader to: * materials design * synthesis * physical properties * emerging applications Carefully selected references round off this well-organized compendium. It is an indispensable guide to experienced researchers in coordination and organometallic chemistry as well as in liquid-crystal and materials science. Newcomers and graduate students will also benefit from this didactically sound introduction to the field.

Quenched-phosphorescence Detection of Molecular Oxygen

Quenched-phosphorescence Detection of Molecular Oxygen PDF Author: Dmitri B Papkovsky
Publisher: Royal Society of Chemistry
ISBN: 1788014553
Category : Science
Languages : en
Pages : 384

Book Description
Significant progress has been made in recent years in quenched-phosphorescence oxygen sensing, particularly in the materials and applications of this detection technology that are open to commercialization, like uses in brain imaging and food packaging. Prompted by this, the editors have delivered a dedicated book that brings together these developments, provides a comprehensive overview of the different detection methodologies, and representative examples and applications. This book is intended to attract new researchers from various disciplines such as chemistry, physics, biology and medicine, stimulate further progress in the field and assist in developing new applications. Providing a concise summary at the cutting edge, this practical guide for current experts and new potential users will increase awareness of this versatile sensing technology.