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Covalent Surface Chemistry of Single‐Walled Carbon Nanotubes

Identifieur interne : 003010 ( Main/Exploration ); précédent : 003009; suivant : 003011

Covalent Surface Chemistry of Single‐Walled Carbon Nanotubes

Auteurs : S. Banerjee [États-Unis] ; T. Hemraj-Benny [États-Unis] ; S. Wong [États-Unis]

Source :

RBID : ISTEX:93F3BF4B348C3CEBAD94AF4E4AE6FA492DC8E4BB

English descriptors

Abstract

In this review article, we explore covalent chemical strategies for the functionalization of carbon‐nanotube surfaces. In recent years, nanotubes have been treated as chemical reagents (be it inorganic or organic) in their own right. Indeed, from their inherent structure, one can view nanotubes as sterically bulky, π‐conjugated ligands, or conversely as electron‐deficient alkenes. Hence, herein we seek to understand, from a structural perspective, the breadth and types of reactions single‐walled nanotubes (SWNTs) can undergo in solution phase, not only at the ends and defect sites but also along the sidewalls. Controllable chemical functionalization suggests that the unique electronic and mechanical properties of SWNTs can be tailored in a determinable manner. Moreover, prevailing themes in nanotube functionalization have been involved with dissolution of tubes.
Single‐walled carbon nanotubes are now considered chemical reagents in their own right. Understanding the reactivity of carbon nanotubes will lead to manipulation of their unique properties in a predictable manner. In this review, reactions leading to functionalization of carbon nanotubes at their ends, at defect sites, and along their sidewalls are discussed with the goal of creating functional nanomaterials with possible device applications and of generating nanoscale hierarchical architectures and assemblies.

Url:
DOI: 10.1002/adma.200401340


Affiliations:


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