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Controlled Covalent Functionalization of 2 H‐MoS 2 with Molecular or Polymeric Adlayers
Author(s) -
QuirósOvies Ramiro,
Vázquez Sulleiro Manuel,
VeraHidalgo Mariano,
Prieto Javier,
Gómez I. Jénnifer,
Sebastián Víctor,
Santamaría Jesús,
Pérez Emilio M.
Publication year - 2020
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202000068
Subject(s) - surface modification , covalent bond , polymer , inert , succinimide , chemical modification , chemistry , molecule , reagent , nanotechnology , materials science , combinatorial chemistry , polymer chemistry , organic chemistry
Most air‐stable 2D materials are relatively inert, which makes their chemical modification difficult. In particular, in the case of MoS 2 , the semiconducting 2 H‐MoS 2 is much less reactive than its metallic counterpart, 1T‐MoS 2 . As a consequence, there are hardly any reliable methods for the covalent modification of 2 H‐MoS 2 . An ideal method for the chemical functionalization of such materials should be both mild, not requiring the introduction of a large number of defects, and versatile, allowing for the decoration with as many different functional groups as possible. Herein, a comprehensive study on the covalent functionalization of 2 H‐MoS 2 with maleimides is presented. The use of a base (Et 3 N) leads to the in situ formation of a succinimide polymer layer, covalently connected to MoS 2 . In contrast, in the absence of base, functionalization stops at the molecular level. Moreover, the functionalization protocol is mild (occurs at room temperature), fast (nearly complete in 1 h), and very flexible (11 different solvents and 10 different maleimides tested). In practical terms, the procedures described here allow for the chemist to manipulate 2 H‐MoS 2 in a very flexible way, decorating it with polymers or molecules, and with a wide range of functional groups for subsequent modification. Conceptually, the spurious formation of an organic polymer might be general to other methods of functionalization of 2D materials, where a large excess of molecular reagents is typically used.