2006
DOI: 10.1016/j.polymer.2005.11.016
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Trialkylsilanes as reagents for the UV-induced surface modification of polybutadiene

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Cited by 28 publications
(29 citation statements)
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“…[8] The distance between the inner face of the front window (made from CaF 2 ) and the sample surface was 7 mm. Polymer films were irradiated either with Hg lamp or a pulsed ArF* excimer laser in the presence of EDMS or gaseous TrMS.…”
Section: Irradiation Experimentsmentioning
confidence: 99%
See 1 more Smart Citation
“…[8] The distance between the inner face of the front window (made from CaF 2 ) and the sample surface was 7 mm. Polymer films were irradiated either with Hg lamp or a pulsed ArF* excimer laser in the presence of EDMS or gaseous TrMS.…”
Section: Irradiation Experimentsmentioning
confidence: 99%
“…The photoassisted introduction of alkylsilyl groups onto polybutadiene surfaces has been studied in detail and it has been found that a hydrogenation of the C C bonds proceeds as a side reaction. [8] In this contribution, we wished to investigate if UV surface modification with trialkylsilanes can be also applied to polymers which do not contain olefinic double bonds. We studied the behavior of the thermoplastic polymer polystyrene (PS) under UVirradiation in presence of UV sensitive trialkylsilanes (EDMS, TrMS).…”
Section: Introductionmentioning
confidence: 99%
“…[3] In a recent contribution, it was demonstrated that trialkysilanes such as trimethylsilane can be used to attach trialkysilyl groups onto the surface of polybutadiene in a UV-assisted hydrosilylation process. [4] In a similar fashion, this process can be applied to derivatives of PPV where the C --C bonds are partly hydrosilylated and partly hydrogenated. [5] Another approach is based upon the thiol-ene reaction: in a radical-mediated reaction, thiols are readily added to C --C groups both in elastomers [6] and derivatives of PPV [7] to give polymers functionalized with alkylthio substituents.…”
Section: Full Papermentioning
confidence: 99%
“…The isomerization is also detectable by the decreasing intensity of the signal at 3 007 cm À1 which stems from C-H stretch vibrations of C --C -H units. [4] Both after 180 and 600 s of UV processing (followed by hydrolysis), the presence of P-OH groups is detectable. The broad IR signals at 2 666 and 2 326 cm À1 are caused by P-OH stretch vibrations.…”
Section: Bromophosphonization Of Polybutadiene and Subsequent Hydrolysismentioning
confidence: 99%
“…The development of modern technologies enables us to create polymer materials with a number of properties which would be impossible to realize in a single polymer. A polymer can acquire special properties either in the course of inter-chain polymer alloying by adding certain monomer units to the basic monomer being polymerized [1] or by modifying the ready-made sample [2][3][4].…”
Section: Introductionmentioning
confidence: 99%