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  • 1
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Organometallic chemistry. ; Chemistry, Organic. ; Electronic books.
    Description / Table of Contents: This Specialist Periodical Report aims to reflect the growing interest in the potential of organometallic chemistry.
    Type of Medium: Online Resource
    Pages: 1 online resource (189 pages)
    Edition: 1st ed.
    ISBN: 9781847558466
    Series Statement: Issn Series
    DDC: 547.05
    Language: English
    Note: Organometallic Chemistry -- CONTENTS -- Preface -- Samarium enolates and their application in organic synthesis -- Samarium enolates-an introduction -- Samarium(II) iodide in organic synthesis -- The formation and use of samarium enolates -- Conclusions -- Metal boryl compounds and metal-catalysed borylation processes: synthetic applications and mechanistic considerations -- Introduction -- Synthesis and reactivity of a novel lithium boryl compound -- Copper boryl complexes and Cu-catalysed borylation reactions -- Copper catalysed reduction of CO2 to CO -- Copper catalysed diboration of aldehydes -- Nucleophilicity of copper boryl complexes-a return -- Diboration of unsaturated carbon-carbon bonds employing Cu, Ag, and Au-NHC systems -- β-boryl elimination processes -- Catalysed borylation of C-H bonds -- Conclusions -- Organometallics in ionic liquids-catalysis and coordination chemistry -- A brief introduction to ionic liquids -- Metal-containing ionic liquids and related salts -- Preparative organometallic chemistry in ionic liquids -- Catalysis with metal complexes in ionic liquids -- Mechanistic investigations -- Spectroscopic investigations -- Concluding remarks -- Groups 1 and 11: the alkali and coinage metals -- Alkali metals -- Copper, silver and gold -- Group 2 (Be-Ba) and Group 12 (Zn-Hg) -- Scope and organisation of the reviews for 2004 and 2005 -- Review of 2004 -- Review of 2005 -- Scandium, yttrium and the lanthanides -- Introduction -- Hydrocarbyls of various kinds -- Allyls -- Cyclopentadienyl-based ancillaries -- COT chemistry -- Carborane-based supporting ligands -- Redox chemistry -- Nitrogen-based ancillary ligand systems -- Organometallics in materials synthesis -- Polymerization chemistry -- Spectroscopy -- Gas phase studies -- Theoretical studies -- Organolanthanides in organic synthesis. , Group 14: silicon, germanium, tin and lead -- Introduction -- A silicon-silicon triple bond -- Other multiply bonded Group 14 compounds -- Aromatic compounds -- Transition metal complexes of heavy Group 14 ligands -- Cyclopentadienyl derivatives -- Organo-transition metal cluster complexes -- Introduction -- Spectroscopic studies -- Theory -- Structural studies -- High-nuclearity clusters -- Group 6 -- Group 8 -- Group 9 -- Group 10 -- Group 11 -- Mixed-metal clusters -- Clusters containing three different metals.
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  • 2
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Organometallic compounds. ; Electronic books.
    Description / Table of Contents: This Specialist Periodical Report aims to reflect the growing interest in the potential of organometallic chemistry.
    Type of Medium: Online Resource
    Pages: 1 online resource (465 pages)
    Edition: 1st ed.
    ISBN: 9781847554208
    Series Statement: Issn Series
    DDC: 547.05
    Language: English
    Note: Organometallic Chemistry -- Contents -- Chapter 1 Theoretical Organometallic Chemistry -- 1 Introduction -- 2 s-Block Metals -- 2.1 Structural, Spectroscopic and Mechanistic Studies -- 3 p-Block Metals -- 3.1 Structural and Spectroscopic Studies -- 3.2 Mechanistic Studies -- 4 d-and f-Block Metals -- 4.1 Structural and Spectroscopic Studies -- 4.2 Mechanistic Studies -- References -- Chapter 2 Groups 1 and 11: The Alkali and Coinage Metals -- 1 Alkali Metals -- 1.1 Introduction -- 1.2 Alkyl Derivatives -- 1.3 Alkenyl, Allyl, Vinyl, Alkynyl and Related Derivatives -- 1.4 Aryl Derivatives -- 1.5 Cyclopentadienyl and Related Derivatives -- 2 Copper, Silver and Gold -- 2.1 Introduction -- 2.2 Copper Compounds -- 2.3 Silver Compounds -- 2.4 Gold Compounds -- References -- Chapter 3 Group 2 (Be-Ba) and Group 12 (Zn-Hg) -- 1 Scope and Organisation of the Review -- 2 Group 2 -- 3 Group 12 -- References -- Chapter 4 Scandium, Yttrium and the Lanthanides -- 1 Introduction -- 2 Synthetic Studies -- 2.1 Cyclopentadienyl Ancillaries -- 2.2 Indenyl, Naphthalene and Other Aromatic π-Complexes -- 2.3 Cyclooctatetraenyl Chemistry -- 2.4 Miscellaneous Ancillaries and Hydrocarbyls -- 3 Organometallics in Materials Synthesis -- 4 Polymerization Chemistry -- 4.1 Non-Polar Mono-Olefin Polymerization -- 4.2 Diene Polymerization -- 4.3 Polymerization of Acrylate Monomers -- 4.4 Polymerization of Lactide -- 5 Spectroscopic and Theoretical Studies -- 6 Lanthanides in Organic Synthesis -- References -- Chapter 5 Carboranes, Including Their Metal Complexes -- 1 Introduction -- 2 Theoretical and Computational Studies -- 3 Carboranes -- 3.1 {CB11} -- 3.2 {C2B8} -- 3.3 {C2B9} -- 3.4 {C2B10} -- 4 Metallacarbaboranes -- 4.1 {MCB10} -- 4.2 {exo-MCB11} -- 4.3 {MC2B8} -- 4.4 {MC2B3} -- 4.5 {MC2B4} and {MC2B8} -- 4.6 {MC2B9} -- 4.7 {exo-MC2B9} -- 4.8 {MC2B10} -- 4.9 {exo-MC2B10}. , 4.10 {MC3B7} -- 5 Biological Carborane Chemistry and BNCT -- 6 Crystal Engineered Supramolecular and Polymeric (Metalla)carborane Materials -- References -- Chapter 6 Group III: B, Al, Ga, In and Tl -- 1 General -- 2 Boron -- 2.1 B(C6F5)3 and Related Boranes -- 2.2 Borate Anions -- 2.3 Boron Hydrides -- 2.4 Boratabenzenes and Related Ligands -- 2.5 Boron-containing Materials -- 2.6 Boron-based Materials -- 2.7 Boron-based Ligand Systems -- 2.8 Boronic Acids -- 2.9 Suzuki and Other Coupling reactions -- 2.10 Diboron(4) Reagents -- 2.11 Borane Functionalized Cyclopentadienyl Ligands -- 2.12 Miscellaneous -- 3 Aluminium -- 3.1 Sub-valent Aluminium and Aluminium Clusters -- 3.2 Aluminoxanes, MAO Models and Aluminium in Olefin Polymerization -- 3.3 Aluminium Derivatives Containing Bonds to Group 15 Elements -- 3.4 Aluminium Derivatives Containing Bonds to Group 16 Elements -- 3.5 Aluminium Organometallics in Organic Synthesis -- 3.6 Miscellaneous Examples -- 4 Gallium -- 4.1 Sub-valent Gallium and Gallium Clusters -- 4.2 Gallium Derivatives Containing Bonds to Group 15 Elements -- 4.3 Gallium Derivatives Containing Bonds to Group 16 Elements -- 4.4 Gallium Organometallics in Organic Synthesis -- 4.5 Gallium Hydrides -- 4.6 Miscellaneous -- 5 Indium -- 5.1 Sub-valent Indium and Indium Clusters -- 5.2 Indium Derivatives Containing Bonds to Groups 15 or 16 -- 5.3 Indium Organometallics in Organic Synthesis -- 5.4 Miscellaneous Examples -- 6 Thallium -- References -- Chapter 7 Group 14: Silicon, Germanium, Tin and Lead -- 1 Overview -- 2 Silylenes and Silyl Anions -- 3 Germylenes, Stannylenes and Plumbylenes -- 4 Multiply Bonded Compounds -- 5 π-Bonded Compounds -- 6 Group 14 Organometallics as Ligands at Transition Metal Centres -- References -- Chapter 8 Group 15: Phosphorus, Arsenic, Antimony and Bismuth -- 1 Phosphorus -- 2 Arsenic -- 3 Antimony. , 4 Bismuth -- References -- Chapter 9 Organic Aspects of Organometallic Chemistry -- 1 Introduction -- 2 Organomagnesium Reagents -- 3 Reactions Involving Organozirconium and Organotitanium Intermediates -- 3.1 Zirconium Species -- 3.2 Titanocene Species -- 3.3 Zirconium and Titanium Allyl Complexes -- 3.4 Alkoxy- and Aryloxy- Titanium and Zirconium Species -- 4 Oxidation and Reduction -- 4.1 Oxidation -- 4.2 Reduction -- 5 Isomerism, Cycloisomerisation, Cyclisation and Cycloaddition -- 5.1 Isomerisation -- 5.2 Cycloisomerisation -- 5.3 Cyclisation -- 5.4 Cycloaddition -- 6 Conjugate Addition and Allylic Substitution Reactions -- 7 Cross Coupling Reactions -- 8 Metathesis -- 8.1 Ring Opening and Ring Closing Metathesis of Alkenes -- 8.2 Cross-Metathesis and Isomerisation of Alkenes -- 8.3 Alkyne Metathesis -- 8.4 Miscellaneous -- 9 Transition Metal Catalysed Hydrodgenation and Hydrometallation -- 9.1 Use of Gaseous Hydrogen and Bidentate Phosphorus Based Ligands -- 9.2 Use of Monodentate Phosphorus Based Ligands -- 9.3 Transfer Hydrogenation -- 9.4 Transition Metal Catalysed Hydroboration, Hydrosilylation and Hydroarylation -- 10 Organozinc and Mai Group Reagents -- 10.1 Organozinc Species -- 10.2 Organoaluminium Reagents -- 10.3 Organotin Reagents -- 10.4 Organobismuth Reagents -- 10.5 Organoboron Reagents -- References -- Chapter 10 Complexes Containing Metal-Carbon σ-Bonds of Groups 4 and 5 (Including Multiple Bonded Species) -- References -- Chapter 11 Complexes Containing Metal-Carbon σ-Bonds of the Group 7 (Including Multiple Bonded Species) -- References -- Chapter 12 Organo-Transition Metal Cluster Complexes -- 1 Introduction -- 2 General Reviews -- 3 Spectroscopic Studies -- 4 Theory -- 5 Structural Studies -- 6 Large Clusters -- 6.1 Homonuclear High-nuclearity Clusters -- 6.2 Heteronuclear High-nuclearity Clusters -- 7 Group 6 -- 8 Group 7. , 8.1 Homometallic Clusters -- 8.2 Mixed-metal Clusters Containing Only Group 7 Metals -- 9 Group 8 -- 9.1 Iron -- 9.2 Ruthenium -- 9.3 Osmium -- 9.4 Mixed-metal Clusters Containing Only Group 8 Metals -- 10 Group 9 -- 10.1 Cobalt -- 10.2 Rhodium -- 10.3 Iridium -- 10.4 Group 9 Clusters as Catalysts -- 11 Group 10 -- 11.1 Nickel -- 11.2 Palladium -- 11.3 Platinum -- 11.4 Mixed-metal Clusters Containing Only Group 10 Metals -- 12 Group 11 -- 12.1 Copper -- 12.2 Silver -- 12.3 Gold -- 13 Mixed-metal Clusters -- 13.1 Group 4 -- 13.2 Group 6 -- 13.3 Group 7 -- 13.4 Group 8 -- 13.5 Group 9 -- 13.6 Group 10 -- 13.7 Group 11 -- 13.8 Clusters Containing Three Different Metals -- References -- Chapter 13 Complexes Containing Metal-Carbon σ-Bonds of the Groups Iron, Cobalt and Nickel, Including Carbenes and Carbynes -- 1 Introduction -- 2 Reviews and Articles of General Interest -- 3 Metal-Carbon s-Bonds Involving Group 8, 9 and 10 Metals -- 3.1 The Iron Triad -- 3.2 The Cobalt Triad -- 3.3 The Nickel Triad -- 4 Carbene and Carbyne Complexes of Groups 8, 9 and 10 -- References -- Chapter 14 Transition Metal Complexes of Cyclopentadienyl Ligands -- 1 General Introduction -- 2 General Chemistry, Main Group, Lanthanides and Actinides -- 3 Titanium, Zirconium and Hafnium -- 4 Vanadium, Niobium and Tantalum -- 5 Chromium, Molybdenum and Tungsten -- 6 Manganese, Rhenium and Technetium -- 7 Iron, Ruthenium and Osmium -- 7.1 Ferrocenes, Ruthenocenes and Osmocenes -- 8 Cobalt, Rhodium and Iridium -- 9 Nickel, Palladium and Platinum -- References.
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  • 3
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Organometallic chemistry. ; Electronic books.
    Description / Table of Contents: A series of critical reviews and perspectives focussing on specific aspects of organometallic chemistry interfacing with other fields of study are provided.
    Type of Medium: Online Resource
    Pages: 1 online resource (165 pages)
    Edition: 1st ed.
    ISBN: 9781849732802
    Series Statement: Issn Series
    DDC: 547.05
    Language: English
    Note: Organometallic Chemistry -- CONTENTS -- Preface -- Synergistic effects in the activation of small molecules by s-block elements -- 1 Introduction -- 2 Historical perspective of bimetallic s-block ates -- 3 Chemistry of alkyl lithium magnesiates -- 4 Chemistry of the turbo-Grignard reagent iPrMgCl·LiCl -- 5 Chemistry of the turbo-Hauser bases (TMP)MgCl·LiCl, (TMP)2Mg·2LiCl and (DA)MgCl·LiCl -- 6 Chemistry of other alkali metal magnesiate complexes -- 7 Conclusions -- References -- Air-stable chiral primary phosphines: part (i) synthesis, stability and applications -- 1 Introduction -- 2 Stability and synthesis -- 3 Applications -- 4 Conclusions -- References -- Open-shell organometallics: reactivity at the ligand -- 1 Introduction -- 2 Ligand redox non-innocence -- 3 Ligand centred radical-type reactivity in open-shell organometallic chemistry and catalysis -- 4 Summary and conclusions -- References -- Alkali/coinage metals - organolithium, organocuprate chemistry -- 1 The alkali metals -- 2 Group 11 -- Abbreviations -- References -- Group 2 (Be-Ba) and Group 12 (Zn-Hg) -- 1 Scope and organisation of the review -- 2 Group 2 -- 3 Group 12 -- References -- Organo-transition metal cluster complexes -- 1 Introduction -- 2 Reviews -- 3 Theory -- 4 High-nuclearity clusters -- 5 Group 8 -- 6 Group 9 -- 7 Group 10 -- 8 Group 11 -- 9 Mixed-metal clusters -- Abbreviations -- References -- Highlights in low-coordinate group 14 organometallic chemistry -- 1 Activation of small molecules with heavy alkynes -- 2 Heavy alkyne chemistry -- 3 The chemistry of compounds with element-element double bonds -- 4 Heavy group 14 elements as ligands to transition metals -- References.
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  • 4
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Organometallic compounds. ; Organometallic chemistry. ; Electronic books.
    Description / Table of Contents: This Specialist Periodical Report aims to reflect the growing interest in the potential of organometallic chemistry.
    Type of Medium: Online Resource
    Pages: 1 online resource (321 pages)
    Edition: 1st ed.
    ISBN: 9781847558503
    Series Statement: Issn Series
    DDC: 547.05
    Language: English
    Note: Organometallic Chemistry -- Contents -- Groups 1 and 11: The Alkali and Coinage Metals -- 1 Alkali Metals -- 1.1 Introduction -- 1.2 Alkyl Derivatives -- 1.3 Alkenyl, Allyl, Vinyl, Alkynyl and Related Derivatives -- 1.4 Aryl Derivatives -- 1.5 Cyclopentadienyl and Related Derivatives -- 2 Copper, Silver and Gold -- 2.1 Introduction -- 2.2 Copper Compounds -- 2.3 Silver Compounds -- 2.4 Gold Compounds -- References -- Group 2 (Be-Ba) and Group 12 (Zn-Hg) -- 1 Scope and Organisation of the Review -- 2 Group 2 -- 3 Group 12 -- References -- Scandium, Yttrium and the Lanthanides -- 1 Introduction -- 2 Hydrocarbyls of Various Kinds -- 3 Half Sandwich Cyclopentadienyl Complexes -- 4 Metallocene Derivatives -- 5 Ansa Metallocene Ligand Chemistry -- 6 Indenyl and Fluorenyl Complexes -- 7 Functionalized Cyclopentadienyls and Related Ligands -- 7.1 Functional Groups with Nitrogen Donors -- 7.2 Functional Groups with Group 16 Donors -- 8 Hydride Complexes -- 9 Allyls -- 10 Cyclo-Octatetraenyl Complexes -- 11 Nitrogen-Donor Ancillaries -- 11.1 Ketiminate Chemistry -- 11.2 Amido Ancillary Groups -- 12 Organophosphorus Supporting Ligands -- 13 Aryloxide Ancillaries -- 14 Compounds with Boron-Based Ligands -- 15 Materials Chemistry -- 16 Applications in Organic Synthesis -- 16.1 Stoichiometric Reactions -- 16.2 Catalysis -- 17 Polymerization Catalysis -- 17.1 Neutral Olefins and Dienes -- 17.2 Acrylate and Polar Monomer Polymerization -- 18 Theoretical and Computational Studies -- 18.1 Structure and Bonding -- 18.3 Agostic Interactions -- 18.4 Interaction of Small Molecules -- 18.5 Calculating Chemical Reactivity -- 18.6 Pretend Molecules -- 19 Spectroscopic Studies -- References -- Carboranes, Including Their Metal Complexes -- 1 Introduction -- 2 Theoretical and Computational Studies -- 3 Heteroboranes, Carboranes and Heterocarboranes -- 3.1 {B3 and B4}. , 3.2 {B8, B9 and B10} -- 3.3 {B12} -- 3.4 {PCB8} -- 3.5 {SB8} -- 3.6 {CB6, CB7, CB8, CB9} -- 3.7 {CB11} -- 3.8 {NC2B7} -- 3.9 {As2C2B7} -- 3.10 {C2B9} -- 3.11 {C2B10} -- 3.12 {C2B11} -- 4 Metallaboranes and Metallacarboranes -- 4.1 {MB3 and MB4} -- 4.2 {MB5} -- 4.3 {MB6 and MB8} -- 4.4 {MCB8} -- 4.5 {MCB9} -- 4.6 {MCB10} -- 4.7 {MC2B4} -- 4.8 {C2B8} -- 4.9 {MC2B9} -- 4.10 {MC2B10} -- 4.11 {MPC2B8} -- 4.12 {M2C3B8} -- 4.13 {exo-C2B9} -- 5 Biological Carborane Chemistry and BNCT -- 6 Weakly Coordinating Anions and Catalysis -- 7 Crystal Engineered Supramolecular and Polymeric (Metalla)carborane Materials -- References -- Group III - B, Al, Ga, In, Tl -- 1 General -- 2 Boron -- 2.1 B(C6F5)3 and Related Boranes -- 2.2 Borate Anions -- 2.3 Ligand Systems Based Around a Tri- or Tetra-Coordinate Boron Centre -- 2.4 Boron Hydrides -- 2.5 Boron-Based Ligand Systems -- 2.6 Boratabenzenes and Related Systems -- 2.7 Boron-Containing Materials and Sensors -- 2.8 Boronic Acids/Esters and Suzuki Type Coupling Reactions -- 2.9 Boron Functionalized Cyclopentadienyl Ligands -- 2.10 Miscellaneous -- 3 Aluminium -- 3.1 Hydrides -- 3.2 Aluminate Complexes -- 3.3 Aluminium Derivatives Containing Bonds to Group 15 Donors -- 3.4 Aluminium Derivatives Containing Bonds to Oxygen -- 3.5 Aluminium Organometallics in Organic Synthesis -- 3.6 Miscellaneous Examples -- 4 Gallium -- 4.1 Subvalent Gallium Species and Clusters -- 4.2 Complexes Containing Subvalent Gallium Species as Ligands -- 4.3 Arylgallium Species -- 4.4 Gallium Hydrides -- 4.5 Gallium Derivatives Containing Bonds to Group 15 or Group 16 Elements -- 4.6 Miscellaneous -- 5 Indium -- 5.1 Subvalent Indium and Indium Clusters -- 5.2 Indium Derivatives Containing Bonds to Groups 15 or 16 -- 5.3 Miscellaneous Examples -- 6 Thallium -- References -- Group 14: Silicon, Germanium, Tin and Lead -- 1 Overview. , 2 Multiple Bonds in Group 14 -- 3 Tetrylenes -- 4 Radicals, Cations and Anions -- 5 Homoaromatics and Other Ring Systems -- 6 π-Bonded Complexes -- 7 Group 14 Organometallics as Ligands at Transition Metal Centres -- References -- Recent Advances in the Chemistry of Phosphaalkynes: Building Blocks for Novel Organophosphorus Compounds -- 1 Introduction -- 2 Synthesis of New Phosphaalkynes -- 3 Phosphagrignard Reagents and Related Compounds -- 4 Synthesis of Four-Membered Rings -- 5 Synthesis of Higher Phosphaalkyne Oligomers -- 6 Synthesis of Cluster Compounds -- 7 Conclusions and Outlook -- References -- Organo-Transition Metal Cluster Complexes -- Abbreviations -- 1 Introduction -- 2 General Reviews -- 3 Spectroscopic Studies -- 4 Theory -- 5 Structural Studies -- 6 High-Nuclearity Clusters -- 6.1 Homonuclear High-Nuclearity Clusters -- 6.2 Heteronuclear High-Nuclearity Clusters -- 7 Group 6 -- 8 Group 7 -- 9 Group 8 -- 9.1 Iron -- 9.2 Ruthenium -- 9.3 Osmium -- 9.4 Mixed-Metal Clusters Containing Only Group 8 Metals -- 9.5 Group 8 Clusters in Catalysis -- 10 Group 9 -- 10.1 Cobalt -- 10.2 Rhodium -- 10.3 Iridium -- 10.4 Group 9 Mixed-Metal Clusters -- 11 Group 10 -- 12 Group 11 -- 13 Mixed-Metal Clusters -- 13.1 Group 5 -- 13.2 Group 6 -- 13.3 Group 7 -- 13.4 Group 8 -- 13.5 Group 9 -- 13.6 Group 10 -- 13.7 Clusters Containing Three Different Metals -- References -- Complexes Containing Metal-Carbon σ-Bonds of the Groups Iron, Cobalt and Nickel, Including Carbenes and Carbynes -- 1 Introduction -- 2 Reviews and Articles of General Interest -- 3 Metal-Carbon σ-Bonds Involving Group 8, 9 and 10 Metals -- 3.1 The Iron Triad -- 3.2 The Cobalt Triad -- 3.3 The Nickel Triad -- 4 Carbene and Carbyne Complexes of Group 8, 9 and 10 -- References -- Organic Aspects of Organometallic Chemistry -- 1 Introduction -- 2 Methods for C-C Bond Formation. , 3 Methods for C-X Bond Formation -- 4 Metal Mediated Cyclisation and Cycloisomerisation Reactions -- 5 Nicholas and Pauson-Khand Type Reactions -- References.
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  • 5
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Organometallic chemistry. ; Chemistry, Organic. ; Electronic books.
    Description / Table of Contents: This Specialist Periodical Report aims to reflect the growing interest in the potential of organometallic chemistry.
    Type of Medium: Online Resource
    Pages: 1 online resource (499 pages)
    Edition: 1st ed.
    ISBN: 9781847558497
    Series Statement: Issn Series
    DDC: 547.05
    Language: English
    Note: Organometallic Chemistry -- Contents -- Chapter 1 Theoretical Organometallic Chemistry -- 1 Introduction -- 2 s- and p-Block Metals -- 2.1 Structural and Spectroscopic Studies -- 2.2 Mechanistic Studies -- 3 d- and f-Block Metals -- 3.1 Structural and Spectroscopic Studies -- 3.2 Mechanistic Studies -- References -- Chapter 2 Groups 1 and 11: The Alkali and Coinage Metals -- 1 Alkali Metals -- 1.1 Introduction -- 1.2 Alkyl Derivatives -- 1.3 Alkenyl, Allyl, Vinyl, Alkynyl and Related Derivatives -- 1.4 Aryl Derivatives -- 1.5 Cyclopentadienyl and Related Derivatives -- 2 Copper, Silver and Gold -- 2.1 Introduction -- 2.2 Copper Compounds -- 2.3 Silver Compounds -- 2.4 Gold Compounds -- References -- Chapter 3 Group 2 (Be-Ba) and Group 12 (Zn-Hg) -- 1 Scope and Organisation of the Review -- 2 Group 2 -- 3 Group 12 -- References -- Chapter 4 Scandium, Yttrium and the Lanthanides -- 1 Introduction -- 2 New Compounds - Structure and Reactivity -- 2.1 Cyclopentadienyl (Cp) and Lightly Substituted Cp Compounds -- 2.2 Cp* and Related Per-substituted Ancillaries -- 2.3 Functionalized Cp Ligands -- 2.4 Linked and Ansa-Cp Ligands -- 2.5 Indenyl and Fluorenyl Ancillaries -- 2.6 Heterocyclic Ancillaries -- 2.7 Amido and other Nitrogen-based Supports -- 2.8 Carborane and other Boron-containing Ligands -- 2.9 Aluminates -- 2.10 Other Ancillaries -- 3 Theoretical Studies -- 4 Gas Phase Chemistry -- 5 Polymerization Catalysis -- 5.1 Olefin Polymerization -- 5.2 Butadiene -- 5.3 Acrylates -- 5.4 Polar Monomers -- 6 Applications in Organic Synthesis -- References -- Chapter 5 Carboranes, Including Their Metal Complexes -- 1 Introduction -- 2 Theoretical and Computational Studies -- 3 Carboranes -- 3.1 {CB8} and {CB9} -- 3.2 {CB10} -- 3.3 {CB11} -- 3.4 {C2B3} -- 3.5 {C2B7} -- 3.6 {C2B8} -- 3.7 {C2B9} -- 3.8 {C2B10} -- 3.9 {C3B3} and {C4B2} -- 4 Metallacarbaboranes. , 4.1 {MCB10} -- 4.2 {exo-MCB11} -- 4.3 {MC2B4} -- 4.4 {MC2B8} -- 4.5 {MC2B9} -- 4.6 {MC2B10} -- 4.7 {exo-MC2B10} -- 5 Biological Carborane Chemistry and BNCT -- 6 Crystal Engineered Supramolecular and Polymeric (Metalla)carborane Materials -- References -- Chapter 6 Group III - B, Al, Ga, In and Tl -- 1 General -- 2 Boron -- 2.1 B(C6F5)3 and Related Boranes -- 2.2 BorateAnions -- 2.3 Boron Hydrides -- 2.4 Boratabenzenes and Related Systems -- 2.5 Boron-containing Materials -- 2.6 Boron-based Sensors -- 2.7 Boron-based Ligand Systems -- 2.8 Boronic Acids and Suzuki Type Coupling Reactions -- 2.9 Diboron(4) Reagents -- 2.10 Borane Functionalized Cyclopentadienyl Ligands -- 2.11 Miscellaneous -- 3 Aluminium -- 3.1 Sub-valent Aluminium and Aluminium Clusters -- 3.2 Aluminoxanes, MAO Models and Aluminium in Olefin Polymerization -- 3.3 Aluminium Derivatives Containing Bonds to Group 15 Elements -- 3.4 Aluminium Derivatives Containing Bonds to Group 16 Elements -- 3.5 Aluminium Organometallics in Organic Synthesis -- 3.6 Miscellaneous Examples -- 4 Gallium -- 4.1 Sub-valent Gallium Species and Clusters -- 4.2 Complexes Containing Subvalent Gallium Species as Ligands -- 4.3 Gallium Derivatives Containing Bonds to Group 15 Elements -- 4.4 Gallium Derivatives Containing Bonds to Group 16 Elements -- 4.5 Gallium Hydrides -- 4.6 Miscellaneous -- 5 Indium -- 5.1 Subvalent Indium and Indium Clusters -- 5.2 Indium Derivatives Containing Bonds to Groups 15 or 16 -- 5.3 Indium Organometallics in Organic Synthesis -- 5.4 Miscellaneous Examples -- 6 Thallium -- References -- Chapter 7 Group 14: Silicon, Germanium, Tin and Lead -- 1 Overview -- 2 Silylenes -- 3 Germylenes, Stannylenes and Plumbylenes -- 4 Multiple Bonds to Main Group Elements -- 5 Homoaromatics and Related Copmpounds -- 6 π-Bonded Compounds -- 7 Transition and Main Group Metal Complexes -- References. , Chapter 8 Group 15: Phosphorus, Arsenic, Antimony and Bismuth -- 1 Phosphorus -- 2 Arsenic -- 3 Antimony -- 4 Bismuth -- References -- Chapter 9 Organo-Transition Metal Cluster Complexes -- 1 Introduction -- 2 General Reviews -- 3 Spectroscopic Studies -- 4 Theory -- 5 Structural Studies -- 6 Large Clusters -- 6.1 Homonuclear High-nuclearity Clusters -- 6.2 Heteronuclear High-nuclearity Clusters -- 7 Group 6 -- 8 Group 7 -- 8.1 Rhenium -- 9 Group 8 -- 9.1 Iron -- 9.2 Ruthenium -- 9.3 Osmium -- 9.4 Mixed-metal Clusters Containing Only Group 8 Metals -- 10 Group 9 -- 10.1 Cobalt -- 10.2 Rhodium -- 10.3 Iridium -- 10.4 Group 9 Mixed Metal Clusters -- 10.5 Group 9 Clusters as Catalysts -- 11 Group 10 -- 11.1 Nickel -- 11.2 Palladium -- 11.3 Platinum -- 12 Group 11 -- 12.1 Copper -- 12.2 Silver -- 12.3 Gold -- 13 Group 12 -- 13.1 Mercury -- 14 Mixed Metal Clusters -- 14.1 Group 5 -- 14.2 Group 6 -- 14.3 Group 7 -- 14.4 Group 8 -- 14.5 Group 9 -- 14.6 Group 10 -- 14.7 Group 11 -- 14.8 Clusters Containing Three Different Metals -- References -- Chapter 10 Complexes Containing Metal-Carbon σ-Bonds of the Groups Iron, Cobalt and Nickel, Including Carbenes and Carbynes -- 1 Introduction -- 2 Reviews and Articles of General Interest -- 3 Metal-Carbon σ-Bonds Involving Group 8, 9 and 10 Metals -- 3.1 The Iron Triad -- 3.2 The Cobalt Triad -- 3.3 The Nickel Triad -- 4 Carbene and Carbyne Complexes of Group 8, 9 and 10 -- References -- Chapter 11 Reactions of Transition Metal π-Complexes of Alkenes, Alkynes and Dienes -- 1 Introduction -- 2 Reviews -- 3 Complexes Containing π-Coordinated Alkenes -- 3.1 Well-defined π-Coordinated Alkenes -- 3.2 π-Coordinated Alkenes Generated In-situ -- 4 Complexes Containing π-Coordinated Alkynes -- 4.1 π-Coordinated Alkynes Generated In-situ -- 5 Complexes Containing π-Coordinated Dienes (Chain and Cyclic). , 5.1 Well-defined π-Coordinated Conjugated Dienes -- 5.2 Well-defined π-Coordinated Non-conjugated Dienes -- 5.3 π-Coordinated Dienes Generated In-situ -- 6 Bimetallic Complexes Containing π-Coordinated Alkenes, Alkynes or Dienes -- 6.1 Homobimetallic -- 6.2 Heterobimetallic -- References -- Chapter 12 Transition Metal Complexes of Cyclopentadienyl Ligands -- 1 General Introduction -- 2 Main Group, Lanthanides and Actinides -- 3 Titanium, Zirconium and Hafnium -- 4 Vanadium, Niobium and Tantalum -- 5 Chromium, Molybdenum and Tungsten -- 6 Manganese, Rhenium and Technetium -- 7 Iron, Ruthenium and Osmium -- 7.1 General Ferrocene and Synthetic Chemistry -- 7.2 Electrochemistry -- 7.3 Polymer Chemistry -- 7.4 Schiff Bases Ligand/Complexes -- 7.5 NMR -- 7.6 Materials Chemistry -- 7.7 Liquid Crystals -- 7.8 Complexes/Coordination -- 7.9 Carbon-based Structures -- 7.10 Dppf as a Ligand -- 7.11 Theoretical -- 7.12 Miscellaneous Ferrocene Chemistry -- 8 Cobalt -- 9 Nickel -- References -- Chapter 13 Organic Aspects of Organometallic Chemistry -- 1 Introduction -- 2 Methods for C-C Bond Formation -- 3 Methods for C-X Bond Formation -- 4 Metathesis Reactions -- 5 Metal Mediated Cyclisation and Cycloisomerisation Reactions -- 6 Metal Mediated Cycloadditions -- 7 Pauson-Khand Type Reactions -- 8 Nicholas Reactions -- References.
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 41 (1976), S. 2963-2965 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Grass and forage science 13 (1958), S. 0 
    ISSN: 1365-2494
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: A leafy strain of timothy and of perennial ryegrass showed no significant reductions in seed yields following grazing at different dates from October to January, when extra nitrogen was applied.Spring and winter + spring grazing, together with extra nitrogen, significantly reduced the seed yield of S50 timothy for three successive harvest years.Perennial ryegrass S101 showed no reduction after spring or winter + spring grazing when defoliation was made not later than mid-April, but when grazing was delayed until May and drought occurred there was a significant reduction in seed yield.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    BJOG 83 (1976), S. 0 
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: This paper reports two randomized control trials on the effects of nalorphine, pethidine, morphine and heroin on fetal and maternal acid base status. The drugs decreased pH and increased pCO2 in the mother, and decreased pH and base excess in the fetus. The changes in the fetus were independent of the changes in the mother. In equivalent dosages, nalorphine increased maternal pCO2 more than pethidine and morphine. The effects of heroin were found to be greater than that of other drugs, and we suggest that heroin should be avoided where the fetus is already at risk.
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  • 9
    ISSN: 1471-0528
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A random controlled trial was performed to compare the effects of the dorsal and left-tilt delivery positions upon fetal acid-base status. The dorsal position was associated with a time-related decrease in fetal pH, whereas the left tilt position was not.
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  • 10
    ISSN: 1745-6584
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: The ability to predict the transport of dissolved gases in the presence of small amounts of trapped gas in an otherwise water-saturated porous medium is needed for a variety of applications. However, an existing model based on equilibrium partitioning of dissolved gas between aqueous and trapped gas phases does not accurately predict the shape of experimentally observed breakthrough and elution curves in column experiments. The objective of this study was to develop and test a kinetic model for dissolved gas transport that combines the advection-dispersion equation with diffusion controlled mass transfer of dissolved gas between the aqueous and trapped gas phases. The model assumes one-dimensional, steady-state ground-water flow, a single dissolved gas component, and a stationary trapped gas phase with constant volume. The model contains three independent parameters: the Peclet number, P, retardation factor, R, and dimensionless mass transfer parameter, ω. The model accurately described the shape of breakthrough and elution curves for dissolved oxygen in column experiments performed with a poorly graded sand and varying amount and composition of trapped gas. Estimated values of P for the bromide tracer increased from 5.92 to 174, corresponding to a decrease in dispersivity from 5.02 to 0.17 cm, as the trapped gas volume increased from 0 to 30% of the pore space. It is speculated that this effect is due to a narrower pore size distribution (and hence more uniform pore scale velocity distribution) caused by trapped gas bubbles selectively occupying the largest pores. Estimated values of R increased from 1 to 13.6 as the trapped gas volume increased and confirmed earlier observations that even small amounts of trapped gas can significantly reduce rates of dissolved oxygen transport. Estimated values of ω ranged from 0.3 to 12.1. Although it was not possible to independently measure mass transfer coefficients or interfacial areas, values computed from flow rates and estimated w values are consistent with values computed by assuming (1) that interfacial area is proportional to trapped gas volume, (2) that trapped gas bubbles are spheres with diameters the same size as soil particles, and (3) that mass transfer is limited by diffusion of dissolved oxygen through water films surrounding trapped gas bubbles.
    Type of Medium: Electronic Resource
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