HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591851Generated: November 2, 2026
N,N,N',N'-Tetramethylethylenediamine → Benzene, ethenyl-, polymer with 1,3-butadiene
https://huagongshe.com/reaction/1591851
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | HCID 71435772 | HCID 71435772 | — |
| Product | Benzene, ethenyl-, polymer with 1,3-butadiene | HCID 62697 | — |
Reaction Steps
The procedure described in Example 1 was utilized in this example except that 1 mL of 1 M solution of sodium alkoxide (NaOR), i.e., sodium mentholate, in hexanes and 1 mL of 1 M solution of N,N,N′,N′-tetramethylethylene diamine (TMEDA) in hexanes were added to the catalyst system (BaTHFA/MgR2) making the molar ratio (BaTHFA/MgR2/NaOR/TMEDA) 1:3:1:1. The styrene-butadiene produced was determined to have a glass transition temperature (Tg) at −77° C. and a melting temperature (Tm) at +8° C. The Mooney viscosity (ML-4) at 100° C. was 89. The GPC measurements indicated that the polymer has a number average molecular weight (Mn) of 284,600 g/mol and a weight average molecular weight (Mw) of 350,800 g/mol. The polydispersity (Mw/Mn) of the resulting polymer was 1.23. Carbon-13 NMR analysis showed a trans 1,4 polybutadiene content of 74.20%, cis 1,4 polybutadiene content of 19.80%, a 1,2 polybutadiene content of 6%, and a polystyrene content of 18%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07291687B1 |
|---|
| Source dataset | uspto-grants-2007_11 |
|---|
| ORD ID | ord-bd95c761b65e4f34af036d1bc28b84fd |
|---|
| Source note | uspto-grants-2007_11 |
|---|