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Boron : sensing, synthesis and supramolecular self-assembly / edited by Meng Li (University of Bath, Bath, UK), John S. Fossey (University of Birmingham, Edgbaston, UK), Tony D. James (University of Bath, Bath, UK)

Contributor(s): Resource type: Ressourcentyp: Buch (Online)Book (Online)Language: English Series: RSC e-book collection | Monographs in supramolecular chemistry ; No. 16Publisher: Cambridge : Royal Society of Chemistry, 2015Copyright date: © 2016Description: 1 Online-Ressource (xxiii, 416 pages) : IllustrationenISBN:
  • 9781782622123
  • 9781782627579
Subject(s): Additional physical formats: 9781849736749 | Erscheint auch als: Boron. Druck-Ausgabe. Cambridge : Royal Society of Chemistry, 2016. xxiii, 416 Seiten | Print version: Boron : Sensing, Synthesis and Supramolecular Self-Assembly. Cambridge : Royal Society of Chemistry,c2015DDC classification:
  • 546/.671 23
RVK: RVK: VK 7719LOC classification:
  • QD181.B1
DOI: DOI: 10.1039/9781782622123Online resources: Summary: 1.5 Structure and Molecular Recognition of Boronic Acid-Containing Polymers1.5.1 Polymers Containing Boronic Acid in the Main-Chain; 1.5.2 Boronic Acid-Appended Polymers; 1.5.3 Self-Assembly of Boronic Acids onto Polymers; 1.6 Boronic Acid-Based Thin Films for Colorimetric Saccharide Sensing; References; Chapter 2 -- 11B NMR and Its Uses in Structural Characterization of Boronic Acids and Boronate Esters; 2.1 Introduction; 2.2 NMR Technique; 2.3 11B NMR Chemical Shifts; 2.4 Tricoordinate Boranes and Trialkylboranes; 2.5 Unsaturation and Heteroatoms in AlkylboranesSummary: 2.6 Boron Compounds with Oxygen Ligands2.7 Borohydrides, Alkylborohydrides and Tetraalkylborates; 2.8 11B NMR in Boronic Acid Systems; 2.9 Conclusions; References; Chapter 3 -- Preparations and Applications of Hexyleneglycol Organoboronic Esters; 3.1 Introduction; 3.1.1 Abbreviations; 3.1.2 Early Work; 3.1.3 Differences in Stability Among Cyclic Boronic Esters; 3.2 Reagents for the Preparation of Organoboronic Esters; 3.2.1 Trialkoxyboranes; 3.2.2 Cyclic Dialkoxyboranes; 3.2.1.1 HBhg; 3.2.2.2 HBpin; 3.2.2.3 HBnpg; 3.2.3 Diboron Reagents; 3.3 Alkylboronic EstersSummary: 3.3.1 Preparations of Hexyleneglycol Alkylboronic Esters3.3.1.1 Hydroboration of Alkenes with HBhg; 3.3.1.2 Enantioselective Rhodium-Catalyzed Hydroboration; 3.3.1.3 Influence of the Diol in Lithiation-Borylation Reactions; 3.3.1.4 Conjugate Addition with Diboron Reagents and Diboration; 3.3.1.5 Boronic Esters from Alkyl Bromides; 3.3.2 Applications of Hexyleneglycol Alkylboronic Esters; 3.3.2.1 Transformation into Alkyltrifluoroborates and Cross-Coupling; 3.3.2.2 Boron to Magnesium Transmetalation; 3.4 Alkenylboronic Esters; 3.4.1 Preparations of Hexyleneglycol Alkenylboronic EstersSummary: 3.4.1.1 2-Vinyl-4,4,6-trimethyl-1,3,2-dioxaborinane3.4.1.2 Hydroboration of Alkynes; 3.4.1.2.1 HBhg.The uncatalyzed hydroboration of alkynes with (hexyleneglycol)borane HBhg was first mentioned by Woods and Strong in 1966.1...; 3.4.1.2.2 Comparison with HBpin.A comparison of the intrinsic reactivity of HBhg and HBpin in this hydroboration was performed by competit...; 3.4.1.3 Miscellaneous; 3.4.1.3.1 Chloroboration of Alkynes.In 2009, a series of new potassium (Z)-2-chloroalk-1-enyltrifluoroborate derivatives were prepared andSummary: Cover; Boron Sensing, Synthesis and Supramolecular Self-Assembly; Preface; Contents; About the Editors; Acknowledgements; Chapter 1 -- Supramolecular Chemistry of Boronic Acids; 1.1 Boronic Acid-Based Organogels; 1.1.1 Low Molecular Weight Gelators; 1.1.2 Polymeric Hydrogels; 1.2 Boronic Acid-Appended Porphyrins; 1.2.1 Monomeric Porphyrins; 1.2.2 Dimeric Porphyrins; 1.3 Interfacial Molecular Recognition by Boronic Acid-Appended Amphiphiles; 1.4 Boronic Acid-Functionalized Metal Nanoparticles; 1.4.1 Gold Nanoparticles; 1.4.2 Other Metal NanoparticlesPPN: PPN: 843850310Package identifier: Produktsigel: ZDB-1-RSEK | ZDB-11-EBC
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