The introduction of silicon substituents can modify the electronic properties of the TTF core. This can lead to changes in the redox behavior, making silylated TTFs useful in organic electronics and charge transport materials.
If you need to purchase chemical raw materials, submit your demand information to get the latest quotations.
Me3TTF(SiPh2H)
{Co(III)(octaethylporphyrin)}radical(2+)(ClO4)2
C77H24O
4,8-bis(4-decylphenylethynyl)benzo[1,2-b:4,5-b']dithiophene
{[2-(benzyloxycarbonyl-benzyloxycarbonylmethyl-amino)-ethyl]-tert-butoxycarbonylmethyl-amino}-acetic acid tert-butyl ester
cis-[PtCl2(1-phenylphosphinane)2]
1-[1-[1-nitro-2-(1H-pyrrol-2-yl)ethyl]cyclohexyl]propanoate
1-(4-(phenylethynyl)phenyl)propyn-3-ol
3,6-bis(4-bromophenyl)-1H,4H-furo[3,4-c]furan-1,4-dione
INDIUM PHOSPHIDE
N-[4-(1,3-dioxo-1,3-dihydroisoindol-2-yl)-2-phenoxyphenyl]methanesulfonamide
Di-(2-furyl)-phenylphosphinoxid
benzyl 4,5-dihydro-3-methylnaphtho<1,2-c>pyrrole-1-carboxylate
N,N'-(4,5-dinitro-1,2-phenylene)bis(4-methylbenzenesulfonamide)
