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Monika J. Sienkowska

Researcher at University of Pennsylvania

Publications -  29
Citations -  2618

Monika J. Sienkowska is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Liquid crystal & Mesophase. The author has an hindex of 18, co-authored 29 publications receiving 2426 citations. Previous affiliations of Monika J. Sienkowska include University of Wrocław & Vanderbilt University.

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Ultrafast synthesis of ultrahigh molar mass polymers by metal-catalyzed living radical polymerization of acrylates, methacrylates, and vinyl chloride mediated by SET at 25 degrees C.

TL;DR: It is reported that polarsolvents such as H(2)O, alcohols, dipolar aprotic solvents, ethylene and propylene carbonate, and ionic liquids instantaneously disproportionate Cu(I)X into Cu(0) and Cu(II)X(2), facilitating an ultrafast LRP in which the free radicals are generated by the nascent and extremely reactive Cu( 0) atomic species.
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Self-Assembly of Janus Dendrimers into Uniform Dendrimersomes and Other Complex Architectures

TL;DR: Dendrimersomes marry the stability and mechanical strength obtainable from polymersomes with the biological function of stabilized phospholipid liposomes, plus superior uniformity of size, ease of formation, and chemical functionalization, providing access to systematic tuning of molecular structure and of self-assembled architecture.
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Synthesis and retrostructural analysis of libraries of AB3 and constitutional isomeric AB2 phenylpropyl ether-based supramolecular dendrimers.

TL;DR: The more flexible and less compact 3-phenylpropyl ether repeat units are stable under acidic conditions, facilitate a simpler synthetic strategy, provide faster dynamics of self- assembly into higher-order supramolecular structures of larger dimensions, exhibit lower transition temperatures than the corresponding benzyl ether homologues, and demonstrate the generality of the self-assembly concept based on amphiphilic dendrons.
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Principles of self-assembly of helical pores from dendritic dipeptides

TL;DR: The results of these investigations together with those of previous studies on the role of dipeptide stereochemistry and protective groups on this self-assembly process provide the molecular principles required to program the construction of supramolecular helical pores with diameter controlled at the A level from a single dendritic diPEptide architecture.
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Programming the internal structure and stability of helical pores self-assembled from dendritic dipeptides via the protective groups of the peptide.

TL;DR: The ability of the protective groups to program the structure of the helical pore reveals the simplest design strategy that complements the more complex strategies based on the architecture of the dendron, the stereochemistry, and theructure of the dipeptide.