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Piotr Pawluć

Researcher at Adam Mickiewicz University in Poznań

Publications -  89
Citations -  1242

Piotr Pawluć is an academic researcher from Adam Mickiewicz University in Poznań. The author has contributed to research in topics: Catalysis & Silylation. The author has an hindex of 19, co-authored 83 publications receiving 949 citations. Previous affiliations of Piotr Pawluć include Wrocław University of Economics & university of lille.

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Markovnikov Hydrosilylation of Alkenes: How an Oddity Becomes the Goal

TL;DR: In this paper, the authors present the current state of this topic and the way it has been achieved, with special emphasis put on the issues still unresolved and prospective directions of development based on the trends present in the literature, but without unnecessary attention to some details of only historical significance.
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Graphene oxide-branched polyethylenimine foams for efficient removal of toxic cations from water

TL;DR: A multiscale analysis of the GO-BPEI nanocomposite provided evidence for the covalent grafting of BPEI on GO and the formation of low crystalline porous foams as mentioned in this paper.
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Ruthenium-catalysed hydrosilylation of carbon–carbon multiple bonds

TL;DR: Ruthenium-based catalysts are generally considered to be efficient catalysts due to their high activity and electron transfer features as mentioned in this paper, and have been used extensively in the hydrosilylation of alkenes and alkynes.
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Graphene Oxide Hybrid with Sulfur–Nitrogen Polymer for High-Performance Pseudocapacitors

TL;DR: Graphene oxide is covalently functionalized with a redox active thiourea-formaldehyde polymer, yielding a multifunctional hybrid system that exhibited specific capacitance as high as 400 F g-1, areal capacitance of 160 mF cm-2, and an energy density of 11.1 mWh cm-3.
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New One-Pot Synthesis of (E)-β-Aryl Vinyl Halides from Styrenes

TL;DR: A new, efficient protocol for the highly stereoselective one-pot synthesis of (E)-beta-aryl vinyl iodides and (E-beta- Daryl vinyl bromides from styrenes based on sequential ruthenium-catalyzed silylative coupling-N-halosuccinimide-mediated halodesilylation reactions is reported.