New stable donor-acceptor dyads for molecular electronics was written by Kondratenko, Mykola;Moiseev, Andrey G.;Perepichka, Dmitrii F.. And the article was included in Journal of Materials Chemistry in 2011.Application In Synthesis of 1-Bromo-6-chlorohexane The following contents are mentioned in the article:
A series of new donor-bridge-acceptor dyads with high chem., electrochem., thermal and conformational stability were synthesized by Stille coupling of oligo(3,4-ethylenedioxy)thiophenes (nEDOTs) and 1,4,5,8-naphthalenetetracarboxydiimide (NDI) building blocks. The mol. design provides for complete separation of HOMO and LUMO orbitals. A thiol functionality allows for selective anchoring of the dyads to metal electrodes, through either the donor or acceptor sides of the mol. The optoelectronic properties of the dyads, both in solution and in self-assembled monolayers on gold, were characterized by electrochem., spectroelectrochem. and UV-Vis absorption/emission spectroscopy and the results were further supported by DFT calculations This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Application In Synthesis of 1-Bromo-6-chlorohexane).
1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Application In Synthesis of 1-Bromo-6-chlorohexane
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics