Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thiophene-2,5-dicarbaldehyde | HCID 587784 | — |
| Edukt | 2,2'-(Thiophene-2,5-diyl)diacetonitrile | HCID 12119796 | — |
| Produkt | 3-Dodecylthiophene | HCID 2733655 | — |
Reaktionsschritte
Heterocycles can also be easily included in the copolymer chain. The literature records the preparation of an insoluble cyano-substituted alternating polymer derived from thiophene-2,5-diacetonitrile and thiophene-2,5-dicarboxaldehyde (Kossmehl, G. Ber. Bunsenges. Phys. Chem., 1979, 83, 417) and copolymers based on the thiophene-2,5-dicarboxaldehyde and 2,5-dimethoxyterephthaldehyde (H. Horhold, Z. Chem., 1972, 12). The bischloromethylation of 3-dodecylthiophene gave the unstable product (17), which was immediately treated with cyanide to give the bisnitrile (18). Alternatively, the bis-aldehyde (19) can be synthesized from (17) in 3 steps in an analogous fashion to before. Condensation of (18) with (7) gave a purple polymer (onset of absorbance of 670 nm).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05514878 |
|---|
| Quelldatensatz | uspto-grants-1996_05 |
|---|
| ORD ID | ord-8dee216498d54aae9cbbe9c167ce86e1 |
|---|
| Quellennotiz | uspto-grants-1996_05 |
|---|