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Search for "polysiloxanes" in Full Text gives 7 result(s) in Beilstein Journal of Organic Chemistry.

Radical chemistry in polymer science: an overview and recent advances

  • Zixiao Wang,
  • Feichen Cui,
  • Yang Sui and
  • Jiajun Yan

Beilstein J. Org. Chem. 2023, 19, 1580–1603, doi:10.3762/bjoc.19.116

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  • , and monomers [127][128][129]. Polysiloxanes are another class of crosslinkable polymers. Modern silicone industry typically uses Pt-catalyzed hydrosilylation to crosslink multi-vinyl polysiloxane with silicon hydride compounds to manufacture silicone rubbers [130]. However, hydrosilylation may also be
  • vinyl groups [132], demonstrating a promising new orientation of radical hydrosilylation. It is noteworthy, that since the 1940s, polysiloxanes were crosslinked via hydrogen abstraction from Si–CH3 and a radical coupling mechanism like polyolefins, vide supra [133]. Irradiation can also lead to the
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Published 18 Oct 2023

Silanediol versus chlorosilanol: hydrolyses and hydrogen-bonding catalyses with fenchole-based silanes

  • Falco Fox,
  • Jörg M. Neudörfl and
  • Bernd Goldfuss

Beilstein J. Org. Chem. 2019, 15, 167–186, doi:10.3762/bjoc.15.17

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  • [47]. Compared to these stable carbon-connected silanediols, the readily accessible alkoxy silanediols undergo fast condensation reactions which often lead to unknown and insoluble polysiloxanes [50][51]. Previously, our group reports syntheses and applications of symmetric biphenyl-2,2`-bisfenchol (5
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Published 18 Jan 2019

Synthesis of bi- and bis-1,2,3-triazoles by copper-catalyzed Huisgen cycloaddition: A family of valuable products by click chemistry

  • Zhan-Jiang Zheng,
  • Ding Wang,
  • Zheng Xu and
  • Li-Wen Xu

Beilstein J. Org. Chem. 2015, 11, 2557–2576, doi:10.3762/bjoc.11.276

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  • low yield when the alkynes or azides were linked directly with a hindered group or an aromatic moiety. In 2012, Xu and co-workers disclosed that both the secondary and primary amine-functionalized polysiloxanes were good ligands for the copper-catalyzed Huisgen reaction of organic azides and alkynes
  • [26]. This applied especially when the reaction was catalyzed by CuCl and mediated by the secondary amine-functionalized polysiloxanes at 0 °C in CH2Cl2, where the symmetrically 5,5’-coupled bitriazole was obtained as the major product (Scheme 9). All the alkynes directly linked with the aromatic
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Published 11 Dec 2015

Convenient preparation of high molecular weight poly(dimethylsiloxane) using thermally latent NHC-catalysis: a structure-activity correlation

  • Stefan Naumann,
  • Johannes Klein,
  • Dongren Wang and
  • Michael R. Buchmeiser

Beilstein J. Org. Chem. 2015, 11, 2261–2266, doi:10.3762/bjoc.11.246

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  • ; polymerization; polysiloxanes; Introduction N-Heterocyclic carbenes (NHCs) [1][2][3] have had a resounding impact on organopolymerization [4][5] during the past fifteen years. Considerable research effort has steadily deepened the mechanistic understanding of the polymerization pathways open to NHCs, while the
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Published 20 Nov 2015

Linkage of α-cyclodextrin-terminated poly(dimethylsiloxanes) by inclusion of quasi bifunctional ferrocene

  • Helmut Ritter,
  • Berit Knudsen and
  • Valerij Durnev

Beilstein J. Org. Chem. 2013, 9, 1278–1284, doi:10.3762/bjoc.9.144

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  • verified by the shifts of the protons in the 1H NMR spectra and in the correlation signals of the 2D ROESY NMR spectra. Keywords: cyclodextrins; ferrocene; host–guest systems; polysiloxanes; supramolecular chemistry; Introduction Polymers containing cyclodextrins (CD) covalently or supramolecularly
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Published 01 Jul 2013

Polysiloxane ionic liquids as good solvents for β-cyclodextrin-polydimethylsiloxane polyrotaxane structures

  • Narcisa Marangoci,
  • Rodinel Ardeleanu,
  • Laura Ursu,
  • Constanta Ibanescu,
  • Maricel Danu,
  • Mariana Pinteala and
  • Bogdan C. Simionescu

Beilstein J. Org. Chem. 2012, 8, 1610–1618, doi:10.3762/bjoc.8.184

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  • interactions. The structure is stable in the 20 to 80 °C domain as proved by the oscillatory and rotational rheological tests. Keywords: cyclodextrins; imidazolium salt; ionic liquid; polyrotaxanes; polysiloxanes; Introduction Ionic liquids (ILs) are environmentally friendly solvents with great potential for
  • , high chain flexibility, good thermal, oxidative and UV stability, high gas permeability, surface activity, hydrophobicity, etc., is the class of polysiloxanes, especially polydimethylsiloxanes [24]. It is worth mentioning that ionic liquids based on polydimethylsiloxane and imidazolium salt groups have
  • polysiloxanes with a pendant imidazolium bromide derivative (PDMS-Im/Br) through a multistep procedure (Scheme 1) as an ionic liquid, which serves as a good solvent for β-CD-polydimethylsiloxane polyrotaxane (PRot). The copolymer PDMS-Im is characterized by a (CH3)2SiO/Im(CH3)SiO molar ratio of 3/1, as
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Published 24 Sep 2012

Conjugated polymers containing diketopyrrolopyrrole units in the main chain

  • Bernd Tieke,
  • A. Raman Rabindranath,
  • Kai Zhang and
  • Yu Zhu

Beilstein J. Org. Chem. 2010, 6, 830–845, doi:10.3762/bjoc.6.92

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  • , respectively. Unfortunately, the effect of the chain length on absorption and emission behaviour was not reported. A study on thermomesogenic polysiloxanes containing DPP units in the main chain was published in 2002 [27]: Investigations on the thermotropic phase behaviour using polarizing microscopy revealed
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Published 31 Aug 2010
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