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Photo-Induced Cage Carbon Functionalization of o-Carboranes.

Record Type:	Electronic resources : Monograph/item
Title/Author:	Photo-Induced Cage Carbon Functionalization of o-Carboranes./
Author:	Ni, Hangcheng.
Description:	1 online resource (222 pages)
Notes:	Source: Dissertations Abstracts International, Volume: 81-05, Section: B.
Contained By:	Dissertations Abstracts International81-05B.
Subject:	Organic chemistry. -
Online resource:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=27662572click for full text (PQDT)
ISBN:	9781392884942

Photo-Induced Cage Carbon Functionalization of o-Carboranes.
Ni, Hangcheng.

Photo-Induced Cage Carbon Functionalization of o-Carboranes. - 1 online resource (222 pages)

Source: Dissertations Abstracts International, Volume: 81-05, Section: B.

Thesis (Ph.D.)--The Chinese University of Hong Kong (Hong Kong), 2019.

Includes bibliographical references

Icosahedral carboranes are boron-carbon molecular clusters with many features such as three-dimensional aromaticity, and high chemical and thermal stability. These make them attractive functional units in boron neuron capture therapy agents as medicine, building blocks for supramolecular design/materials, and versatile ligands in coordination/ organometallic chemistry. Despite a wide variety of methodologies developed for the synthesis of functionalized carboranes, development of new methodologies for the synthesis of versatile carborane derivatives in a mild, efficient and cheap way is still demanding.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023

Mode of access: World Wide Web

ISBN: 9781392884942Subjects--Topical Terms:

523952
Organic chemistry.
Subjects--Index Terms:

CarboranesIndex Terms--Genre/Form:

542853
Electronic books.

Photo-Induced Cage Carbon Functionalization of o-Carboranes.
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245 1 0 $a Photo-Induced Cage Carbon Functionalization of o-Carboranes.
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504 $a Includes bibliographical references
520 $a Icosahedral carboranes are boron-carbon molecular clusters with many features such as three-dimensional aromaticity, and high chemical and thermal stability. These make them attractive functional units in boron neuron capture therapy agents as medicine, building blocks for supramolecular design/materials, and versatile ligands in coordination/ organometallic chemistry. Despite a wide variety of methodologies developed for the synthesis of functionalized carboranes, development of new methodologies for the synthesis of versatile carborane derivatives in a mild, efficient and cheap way is still demanding.
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538 $a Mode of access: World Wide Web
650 4 $a Organic chemistry. $3 523952
653 $a Carboranes
653 $a Cage carbon
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773 0 $t Dissertations Abstracts International $g 81-05B.
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