Deposits of clastic carbonate-dominated (calciclastic) sedimentary slope systems in the rock record have been identified mostly as linearly-consistent carbonate apron deposits, even though most ancient clastic carbonate slope deposits fit the submarine fan systems better. Calciclastic submarine fans are consequently rarely described and are poorly understood. Subsequently, very little is known especially in mud-dominated calciclastic submarine fan systems. Presented in this study are a sedimentological core and petrographic characterisation of samples from eleven boreholes from the Lower Carboniferous of Bowland Basin (Northwest England) that reveals a >250 m thick calciturbidite complex deposited in a calciclastic submarine fan setting. Seven facies are recognised from core and thin section characterisation and are grouped into three carbonate turbidite sequences. They include: 1) Calciturbidites, comprising mostly of highto low-density, wavy-laminated bioclast-rich facies; 2) low-density densite mudstones which are characterised by planar laminated and unlaminated muddominated facies; and 3) Calcidebrites which are muddy or hyper-concentrated debrisflow deposits occurring as poorly-sorted, chaotic, mud-supported floatstones. These

Phd by thesis

J. Appl. Cryst.の発刊に際して

Lanthanide ions possess fascinating optical properties and their discovery, first industrial uses and present high technological applications are largely governed by their interaction with light. Lighting devices (economical luminescent lamps, light emitting diodes), television and computer displays, optical fibres, optical amplifiers, lasers, as well as responsive luminescent stains for biomedical analysis, medical diagnosis, and cell imaging rely heavily on lanthanide ions. This critical review has been tailored for a broad audience of chemists, biochemists and materials scientists; the basics of lanthanide photophysics are highlighted together with the synthetic strategies used to insert these ions into mono- and polymetallic molecular edifices. Recent advances in NIR-emitting materials, including liquid crystals, and in the control of luminescent properties in polymetallic assemblies are also presented. (210 references.)

Taking advantage of luminescent lanthanide ions

The development in the field of coordination polymers or metal-organic coordination networks, MOCNs (metal-organic frameworks, MOFs) is assessed in terms of property investigations in the areas of catalysis, chirality, conductivity, luminescence, magnetism, spin-transition (spin-crossover), non-linear optics (NLO) and porosity or zeolitic behavior upon which potential applications could be based.

/pdf/engineering-coordination-polymers-towards-applications-3joywh2v74.pdf

Engineering coordination polymers towards applications

The synthesis and photophysical study of a family of cyclometalated iridium(III) complexes are reported. The iridium complexes have two cyclometalated (C∧N) ligands and a single monoanionic, bidentate ancillary ligand (LX), i.e., C∧N2Ir(LX). The C∧N ligands can be any of a wide variety of organometallic ligands. The LX ligands used for this study were all β-diketonates, with the major emphasis placed on acetylacetonate (acac) complexes. The majority of the C∧N2Ir(acac) complexes phosphoresce with high quantum efficiencies (solution quantum yields, 0.1−0.6), and microsecond lifetimes (e.g., 1−14 μs). The strongly allowed phosphorescence in these complexes is the result of significant spin−orbit coupling of the Ir center. The lowest energy (emissive) excited state in these C∧N2Ir(acac) complexes is a mixture of 3MLCT and 3(π−π*) states. By choosing the appropriate C∧N ligand, C∧N2Ir(acac) complexes can be prepared which emit in any color from green to red. Simple, systematic changes in the C∧N ligands, whic...

Highly phosphorescent bis-cyclometalated iridium complexes: synthesis, photophysical characterization, and use in organic light emitting diodes.

The dynamics of the high-spin→low-spin intersystem crossing process in iron(?) spin-crossover compounds are strongly influenced by cooperative effects of elastic origin which are due to the large difference in volume between high-spin and low-spin complexes. The deviation from first order kinetics is attributed to a build-up of an internal pressure as the relaxation proceeds, leading to a characteristic self-acceleration. The elastic interactions may lead to a light-induced bistability for systems which otherwise remain in the high-spin state down to cryogenic temperatures.

Intersystem Crossing and Light-Induced Bistability in Iron(?) Spin-Crossover Compounds

Spin‐Crossover Materials. Properties and Applications. Herausgegeben von Malcolm A. Halcrow.

Energy transfer between different Eu2+ ions in the white phosphor Ba7F12Cl2:Eu2+

Size-controlled micro- and nanocrystals of a [Ru(bpy)3][NaCr(ox)3] coordination network are prepared using reverse micelles. Compared with the bulk reference, the 2E emission of the Cr(III) ions indicates an efficient directional energy migration toward the surface of the nanocrystals.

Directional Energy Migration in Nanoparticles of Crystalline Metal Complexes

A Pt(II) complex with both a phenanthroline and a tetrathiafulvalene-extended dithiolate ligand: Synthesis, crystal structure, electrochemical and spectroscopic properties

Andreas Hauser

Papers

Intersystem Crossing and Light-Induced Bistability in Iron(?) Spin-Crossover Compounds

Spin‐Crossover Materials. Properties and Applications. Herausgegeben von Malcolm A. Halcrow.

Energy transfer between different Eu2+ ions in the white phosphor Ba7F12Cl2:Eu2+

Directional Energy Migration in Nanoparticles of Crystalline Metal Complexes

A Pt(II) complex with both a phenanthroline and a tetrathiafulvalene-extended dithiolate ligand: Synthesis, crystal structure, electrochemical and spectroscopic properties