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Functionalization of Carborane via Carboryne Intermediates

English · Hardback

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This thesis focuses on the development of new methods of functionalizing carboranes using o-carboryne intermediates. Functional carboranes are now finding a broad range of applications, including organic synthesis, drug design, polymers, catalysis, metal-organic frameworks, electronic devices and more. However, the limited number of efficient synthetic methods for obtaining functional carborane materials has restricted their applications. The methodologies established in this thesis represent simple, yet powerful strategies to assemble previously inaccessible, useful complex molecules, which will also have a significant impact on future synthetic, cluster and materials chemistry. Moreover, it discusses the first method for the in situ generation of electrophilic boron radical using photocatalysis.  

List of contents

Introduction.- Regioselective Insertion of -Carborynes into -C-H Bond of Tertiary Amines.- Synthesis of Carborane-Functionalized Heterocycles: Dearomative [2 + 2] Cycloaddition and sp2 C-H Insertion Reaction.- Reaction of -Carboryne with Nitrones: A Formal [5 + 2] Cycloaddition.- 1,3-Dehydro- -Carborane: Generation and Reaction with Arenes.- Ene Reaction of 1,3-Dehydro- -Carborane.- Cage Boron Arylation of -Carborane via Metal-Free, Visible-Light-Mediated Radical Coupling.- Conclusion.- Experimental Section.

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Summary

This thesis focuses on the development of new methods of functionalizing carboranes using o-carboryne intermediates. Functional carboranes are now finding a broad range of applications, including organic synthesis, drug design, polymers, catalysis, metal−organic frameworks, electronic devices and more. However, the limited number of efficient synthetic methods for obtaining functional carborane materials has restricted their applications. The methodologies established in this thesis represent simple, yet powerful strategies to assemble previously inaccessible, useful complex molecules, which will also have a significant impact on future synthetic, cluster and materials chemistry. Moreover, it discusses the first method for the in situ generation of electrophilic boron radical using photocatalysis.  

Product details

Authors Da Zhao
Publisher Springer, Berlin
 
Languages English
Product format Hardback
Released 01.01.2016
 
EAN 9789811015687
ISBN 978-981-10-1568-7
No. of pages 170
Dimensions 167 mm x 242 mm x 15 mm
Weight 431 g
Illustrations XVII, 170 p. 126 illus., 5 illus. in color.
Series Springer Theses
Springer Theses
Subjects Natural sciences, medicine, IT, technology > Chemistry > Organic chemistry

B, ORGANIC CHEMISTRY, Catalysis, Chemistry and Materials Science, Physical Chemistry

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