Synthesis of a disulfide functionalized diacetylenic derivative of carbazole as building-block of polymerizable self-assembled monolayers

2014 ◽  
Vol 68 (2) ◽  
Author(s):  
Sushilkumar Jadhav ◽  
Massimo Maccagno

AbstractA new symmetrical disulfide containing a diacetylenic unit and bearing a fluorescent carbazolyl end-group forming polymerizable self-assembled monolayers on metallic nanostructures has been synthesized. Suitable modifications of the synthetic steps involved in the synthesis of such derivatives were made in order to assure better synthetic pathway. Conversion of the tosylated derivative into the final symmetrical disulfide is carried out using sodium hydrosulfide (NaSH).

1997 ◽  
Vol 36 (1-4) ◽  
pp. 119-122 ◽  
Author(s):  
J. Collet ◽  
M. Bonnier ◽  
O. Bouloussa ◽  
F. Rondelez ◽  
D. Vuillaume

CrystEngComm ◽  
2020 ◽  
Vol 22 (14) ◽  
pp. 2425-2428
Author(s):  
Harry Pinfold ◽  
Graham Pattison ◽  
Giovanni Costantini

Fluorination turns a prototypical diphenol into an effective hydrogen-bond-donating building block for the formation of 2D phenol–pyridine cocrystals.


2012 ◽  
Vol 1451 ◽  
pp. 179-184
Author(s):  
Cecilia Mattevi ◽  
Florian Colléaux ◽  
Hokwon Kim ◽  
Manish Chhowalla ◽  
Thomas D. Anthopoulos

ABSTRACTWe demonstrate low operating voltage (<|1.5| V) chemical vapour deposited (CVD) graphene transistors using solution processable organic self-assembled monolayers (SAMs) as nanodielectrics. The transistors show weak extrinsic doping, hysteresis-free operation, low gate-leakage current and good operating stability with bias-stress free characteristics. Most importantly we demonstrate that the Dirac potential can be finely tuned by modifying the molecular end-group of the SAMs without compromising the electrical characteristics of the transistors.


1995 ◽  
Vol 99 (18) ◽  
pp. 7102-7107 ◽  
Author(s):  
H. Wolf ◽  
H. Ringsdorf ◽  
E. Delamarche ◽  
T. Takami ◽  
H. Kang ◽  
...  

1997 ◽  
Vol 488 ◽  
Author(s):  
J. Collet ◽  
D. Vuillaume ◽  
M. Bonnier ◽  
O. Bouloussa ◽  
F. Rondelez ◽  
...  

AbstractWe have previously demonstrated that a self-assembled monolayer (SAM) of alkyltrichlorosilane molecules, covalently bonded to the native oxide of a silicon substrate, allows the fabrication of MIS (Metal-Insulator-Semiconductor) devices with excellent electrical properties [1]. Here we demonstrate that we can functionalize, with π-electron moieties, the end-groups of the molecules, once grafted to the substrate, without disturbing the low conductivity through the SAM (σ⊥), while strongly increasing the in-plane conductivity (σ//). The functionalization of the monolayer is monitored by FTIR, ellipsometry and X ray reflectivity. Conductivity, photoconductivity and capacitance measurements are carried out to study the effect of these chemical functionalizations on the electrical properties of the monolayers. We demonstrate that the low perpendicular conductivity (σ⊥≈10−15 S/cm) is not altered by the end-group functionalities while high anisotropic conductivities (σ///σ⊥ ≈ 107-108) are obtained at a monolayer level. Interfacial (Si/SAM and SAM/metal) energy barriers are investigated as a function of the end-group functionalities. We also show that conducting monomers substituted by alkyl chains (3,6- dibromocarbazole-N-octyltrimethoxysilane), directly grafted to the substrate, exhibit similar behavior.


ACS Nano ◽  
2011 ◽  
Vol 6 (1) ◽  
pp. 897-903 ◽  
Author(s):  
Jinne Adisoejoso ◽  
Kazukuni Tahara ◽  
Shengbin Lei ◽  
Paweł Szabelski ◽  
Wojciech Rżysko ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document