Preparation and Properties of Rubberlike High Polymers. II. Polymerization of Mixtures in Bulk

1947 ◽  
Vol 20 (2) ◽  
pp. 380-391
Author(s):  
C. Koningsberger ◽  
G. Salomon

Abstract Mixtures of butadiene and dimethylbutadiene with varying quantities of styrene and acrylonitrile were copolymerized under various catalytic conditions at 100° C. The formation of cyclic dimers from dienes and vinyl compounds is, in some cases, much more pronounced than the dimerization of the dienes alone. Since the latter is also a kind of Diels-Alder reaction, a series with increasing dienophilic properties can be established from a comparison of the yields of cyclic dimers. From solubility and swelling experiments it is evident that the polymers prepared from butadiene and the vinyl compounds and those from dimethylbutadiene and acrylonitrile are true copolymers. The mechanical properties of the copolymers from butadiene and increasing amounts of a vinyl compound change gradually from those of a rubber to those of the polyvinyl compound. The copolymers from a mixture containing 30 per cent styrene or acrylonitrile are very similar to Buna-S and Perbunan, respectively. Copolymers of the same composition from dimethylbutadiene and acrylonitrile, on the other hand, form a new class of thermoplastics with a much higher temperature of elasticity.

1990 ◽  
Vol 68 (3) ◽  
pp. 404-411 ◽  
Author(s):  
Gervais Bérubé ◽  
Pierre Deslongchamps

The syntheses of the acyclic triene trans–trans–cis27 and trans–trans–trans31 are described. Macrocyclization and concomitant transannular Diels–Alder reaction were performed with the chloride derivative obtained from the trans–trans–cis triene alcohol 27 yielding a mixture of the tricyclic compounds trans–syn–trans33 and cis–syn–cis34. On the other hand, macrocyclization of the chloride derived from trans–trans–trans triene 31 was not successful. Keywords: transannular process, Diels–Alder reaction, macrocyclic triene, macrocyclization, tricyclic compounds, organic synthesis.


1990 ◽  
Vol 68 (12) ◽  
pp. 2137-2143 ◽  
Author(s):  
Yao-Chang Xu ◽  
Michel Cantin ◽  
Pierre Deslongchamps

The syntheses of the acyclic dienynes 14a (cis-trans-acetylene) and 14b (trans-trans-acetylene) are described. The tandem macrocyclization and transannular Diels–Alder reaction of the allylic chloride 14b was conducted in the presence of Cs2CO3 at 85 °C in one-pot to provide tricyclic product 16, with the two hydrogens in ring B being cis. On the other hand, treatment of the allylic chloride 14a under the same conditions afforded 14-membered macrocycle 17, which could be transformed at 250 °C into a similar tricyclic product 18 with the two hydrogens in ring B being trans, along with an interesting by-product 19. The mechanism for the formation of 19 is also discussed. Keywords: stereocontrolled synthesis, macrocycle, tricyclic compound, transannular Diels–Alder reaction.


Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1510
Author(s):  
Marek Pöschl ◽  
Shibulal Gopi Sathi ◽  
Radek Stoček ◽  
Ondřej Kratina

The rheometer curing curves of neat natural rubber (NR) and neat chloroprene rubber (CR) with maleide F (MF) exhibit considerable crosslinking torque at 180 °C. This indicates that MF can crosslink both these rubbers via Alder-ene reactions. Based on this knowledge, MF has been introduced as a co-crosslinking agent for a 50/50 blend of NR and CR in conjunction with accelerated sulfur. The delta (Δ) torque obtained from the curing curves of a blend with the addition of 1 phr MF was around 62% higher than those without MF. As the content of MF increased to 3 phr, the Δ torque was further raised to 236%. Moreover, the mechanical properties, particularly the tensile strength of the blend with the addition of 1 phr MF in conjunction with the accelerated sulfur, was around 201% higher than the blend without MF. The overall tensile properties of the blends cured with MF were almost retained even after ageing the samples at 70 °C for 72 h. This significant improvement in the curing torque and the tensile properties of the blends indicates that MF can co-crosslink between NR and CR via the Diels–Alder reaction.


2017 ◽  
Vol 8 (13) ◽  
pp. 2087-2092 ◽  
Author(s):  
Gayan A. Appuhamillage ◽  
John C. Reagan ◽  
Sina Khorsandi ◽  
Joshua R. Davidson ◽  
Walter Voit ◽  
...  

We demonstrate that uniform mechanical properties can be achieved in 3D printed polymer blends by using a dynamic Diels–Alder reaction.


ChemInform ◽  
2015 ◽  
Vol 46 (45) ◽  
pp. no-no
Author(s):  
Jake R. Zimmerman ◽  
Olivia Johntony ◽  
Daniel Steigerwald ◽  
Cody Criss ◽  
Brian J. Myers ◽  
...  

2020 ◽  
Author(s):  
Viola Kolaříková ◽  
Markéta Rybáčková ◽  
Martin Svoboda ◽  
Jaroslav Kvíčala

Prochiral 4-(allyloxy)hepta-1,6-diynes, optionally modified in the positions 1 and 7 with an alkyl or ester group, undergo chemoselective ring closing enyne metathesis yielding racemic 4-alkenyl-2-alkynyl-3,6-dihydro-2H-pyrans. Among the catalysts tested, Grubbs 1st generation precatalyst in the presence of ethene (Mori conditions) gave superior results compared to more stable Grubbs or Hoveyda-Grubbs 2nd generation precatalysts. This is probably caused by suppression of subsequent side-reactions of the enyne metathesis product with ethene. On the other hand, 2nd generation precatalysts gave better yields in the absence of ethene. The metathesis products, containing both triple bond and conjugated system, can be successfully orthogonally modified. For example, metathesis product of 5-(allyloxy)nona-2,7-diyne reacted chemo- and stereoselectively by Diels-Alder reaction with N-phenylmaleimide affording tricyclic products as the mixture of two separable diastereoisomers, the configuration of which was estimated by DFT computations. The reported enediyne metathesis paves the way to enantioselective enyne metathesis yielding chiral building blocks for compounds with potential biological activity, e.g. norsalvinorin or cacospongionolide B.


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