METHOD FOR SYNTHESIZING THIOPHENES
Process for preparing thiophenes useful for the preparation of semiconductive polymers or semiconductive oligomers with a defined mean molar mass and a narrow molecular mass distribution.
1 . Process for preparing oligo- or polythiophenes, comprising the process steps of:
1. reacting at least one dissolved thiophene derivative having two leaving groups to give a polymerization-active monomer by
a) mixing a solution of at least one dissolved thiophene derivative having two leaving groups with a solution of an organometallic compound or
b) reacting a solution of at least one dissolved thiophene derivative having two leaving groups with elemental metal
2. polymerizing the product solution from 1 by the metered addition of a solution of at least one catalyst
3. polymerizing the product solution from 2 by the metered addition of at least one further solution prepared according to 1 to achieve a chain extension based on the same thiophene derivative and/or at least one other thiophene derivative.
2 . Process according to claim 1 , wherein at least one of the process steps of
reacting the solution with at least one thiophene derivative having two leaving groups with an organometallic compound according to step 1 a),
reacting the solution with at least one thiophene derivative having two leaving groups by providing a metal according to step 1 b),
performing the polymerization by the reaction of polymerization-active monomers formed from thiophene derivatives having two leaving groups with a catalyst solution comprising at least one catalyst according to step 2 and/or
continuing the polymerization by at least one addition of further identical polymerization-active monomer or at least one different polymerization-active monomer according to step 3
is conducted continuously.
3 . Process according to claim 1 , wherein that the at least one catalyst according to step 2 is activated in the first metered addition step with 1 to 3 molar equivalents of polymerization-active monomer formed from thiophene derivative having two leaving groups.
4 . Continuous process for preparing oligo- or polythiophenes, comprising the process steps of:
I. continuously converting at least one dissolved thiophene derivative having two leaving groups to a polymerization-active monomer by
a) mixing a solution of at least one dissolved thiophene derivative having two leaving groups with a solution of an organometallic compound or
b) flowing a solution of at least one dissolved thiophene derivative having two leaving groups through or over elemental metal in an apparatus initially charged with the elemental metal,
II. continuously polymerizing the product solution from I after metered addition of a solution of at least one catalyst.
5 . Process according to claim 4 , wherein, after step II, in a step III, the continuous polymerization of the product solution from II is continued by the metered addition of at least one further solution prepared according to I with the purpose of a chain extension based on the same thiophene derivative and/or at least one other thiophene derivative.
6 . Process according to claim 4 , wherein the at least one catalyst is activated with 1 to 3 molar equivalents of polymerization-active monomer formed from thiophene derivative with two leaving groups.
7 . Process according to claim 4 , wherein the apparatus utilized for the continuous process are micromixers, microreactors and micro-heat exchangers.
8 . Process according to claim 1 , wherein a narrow molecular weight distribution of the poly- or oligothiophene having a polydispersity index of 1 to 3 is achieved.
9 . Process according to claim 1 , wherein at least one Pd or Ni catalyst is used.
10 . Process according to claim 1 , wherein the at least one thiophene derivative having two leaving groups is one of the formula:
where
R. at the 3 or 4 position is H or an organic group, and
X and X′ are each independently a leaving group.
11 . Process according to claim 1 , wherein the organometallic compounds include Grignard compounds of the formula R—Mg—X
where R is C 1 , C 2 , C 3 , C 4 , C 5 , C 6 , C 7 , C 8 , C g , C 10 , C 11 , or C 12 -alkyl, and
X is halogen, and
the metal to be provided is magnesium or zinc.
12 . Process according to claim 1 , wherein the solvent used comprises at least one ether component.
13 . Process according to claim 1 , wherein the process is performed within a temperature range of +20 to +200° C. and a pressure of 1-30 bar.
14 . The process of claim 10 , wherein R is an organic group and said organic group is a non-reactive group or a protecting group.
15 . The process of claim 10 , wherein X and X′ are halogen.
16 . The process of claim 15 , wherein said halogen is Cl, Br or I.
17 . The process of claim 16 , wherein said halogen is Br.