Sven Brandau

Acrylonitrile-Butadiene Rubber (NBR) Prepared via Living/Controlled Radical Polymerization (RAFT)

In the current work we present results on the controlled/living radical copolymerization of acrylonitrile (AN) and 1,3-butadiene (BD) via reversible addition fragmentation chain transfer (RAFT) polymerization techniques. For the first time, a solution polymerization process for the synthesis of nitrile butadiene rubber (NBR) via the use of dithioacetate and trithiocarbonate RAFT agents is described. It is demonstrated that the number average molar mass,

High molecular weight acrylonitrile–butadiene architectures via a combination of RAFT polymerization and orthogonal copper mediated azide–alkyne cycloaddition

\overline M _{\rm n}

Determining the Mark–Houwink parameters of nitrile rubber: a chromatographic investigation of the NBR microstructure

, of the NBR can be varied between a few thousand and 60 000 g · mol(-1) with polydispersities between 1.2 and 2.0 (depending on the monomer to polymer conversion). Excellent agreement between the experimentally observed and the theoretically expected molar masses is found. Detailed information on the structure of the synthesized polymers is obtained by variable analytical techniques such as infrared spectroscopy (IR), nuclear magnetic resonance (NMR) spectroscopy, differential scanning calorimetry, and electrospray ionization-mass spectrometry (ESI-MS).

Photo-induced ligation of acrylonitrile-butadiene rubber: Selective tetrazole-ene coupling of chain-end-functionalized copolymers of 1,3-butadiene

α-Functional nitrile butadiene rubber (NBR) building blocks were employed in the copper mediated 1,3-dipolar Huisgen coupling upon addition of 1,4-bis(azidomethyl)benzene (4). Polymer–polymer coupling afforded linear polymers with molecular weights ranging from 2500 g mol−1 to 97 000 g mol−1 and polydispersities from 1.1 to 1.6. The α-functional NBR building blocks were obtained via the reversible addition–fragmentation chain transfer (RAFT) copolymerization of acrylonitrile (AN) and 1,3-butadiene (BD) at 100 °C, utilizing the high temperature azo initiator 1,1′-azobis(cyclohexane-1-carbonitrile) and chlorobenzene or acetone as solvents. A novel alkyne-functional trithiocarbonate 2 was synthesized in 64% yield via the N,N′-dicyclohexylcarbodiimide mediated coupling of 2-((dodecylsulfanyl)carbono-thioyl)sulfanyl propanoic acid (DoPAT, 1) and propargyl alcohol. 2 was shown to be an efficient controlling agent for the controlled/living radical copolymerization of acrylonitrile and 1,3-butadiene. The use of copper mediated azide–alkyne cycloaddition was extended towards the side-chain modification of acrylonitrile–butadiene rubbers as well as applied in the synthesis of branched and cross-linked NBR structures. For this purpose an acrylonitrile-1,3-butadiene–propargyl methacrylate (PMA) terpolymer of 3900 g mol−1 with a PDI of 1.3 was synthesized by a DoPAT-mediated RAFT polymerization. Herein, monomers were employed in the ratio of 56 : 35 : 9 (BD : AN : PMA). The ability of the terpolymer to undergo side-chain modification was demonstrated upon addition of 1-undecane azide. Cross-links were established via addition of 1,4-bis(azidomethyl)benzene. The current study provides the first successful approach to employ an orthogonal conjugation technique on this technically important class of synthetic rubbers.

Mild and Efficient Modular Synthesis of Poly(acrylonitrile-co-butadiene) Block and Miktoarm Star Copolymer Architectures

The microstructure of acrylonitrile–butadiene rubber (NBR) was shown to be dependent on the polymerization conditions. The NBR investigated in the current study was obtained via radical copolymerization under azeotropic conditions (AN/BD = 38/62) in organic solution in the presence of either a conventional chain transfer agent or a reversible addition fragmentation chain transfer (RAFT) agent. The variation in the polymer microstructure was proven to originate from different radical environments during the polymerizations with initial radical initiator concentrations in the polymerizations studied ranging from 1.0 mM to 34.1 mM. The variation of the polymer microstructure was evidenced by triple SEC measurements, making use of the simultaneous determination of molecular weights with two independent methods, namely on-line viscometry and on-line light scattering. It is additionally evidenced that the microstructure shows a gradual variation during the course of a polymerization, a behaviour observed when the polymerizations were performed in the presence of an elevated initial radical initiator concentration. Furthermore, experimental evidence for the variation of the NBR microstructure during RAFT polymerizations is provided. At low conversions, a rather uniform polymer is obtained. With increasing conversion, a loss of the controlled character is observed and the microstructures approach those of nitrile rubber obtained by conventionally controlled free radical copolymerizations employing mercaptane transfer agents. Despite the differences in the polymer microstructure, it is possible to report a single set of MHKS parameters for the prepared NBR with azeotropic composition. A linear regression of the Mark–Houwink plots of the samples polymerized under different conditions gives values of K = (49.5 ± 5.5) × 10−5 dL g−1 and α = 0.689 ± 0.010 with a low error margin for SEC separation in THF at 25 °C. Weight average molecular weights of the investigated NBR samples were in the range of 40000 to 155000 g mol−1. The molecular weights of the copolymers determined via universal calibration with the MHKS parameters presented in the current study show a good agreement with molecular weights obtained from light scattering, underpinning the veracity of the obtained parameters.