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Tania Neva

Researcher at University of Seville

Publications -  5
Citations -  48

Tania Neva is an academic researcher from University of Seville. The author has contributed to research in topics: Supramolecular chemistry & Folding (chemistry). The author has an hindex of 4, co-authored 4 publications receiving 27 citations. Previous affiliations of Tania Neva include Spanish National Research Council.

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Journal ArticleDOI

Tuning the Topological Landscape of DNA-Cyclodextrin Nanocomplexes by Molecular Design.

TL;DR: Original molecular vectors that ensure broad flexibility to tune the shape and surface properties of plasmid DNA (pDNA) condensates are reported that provide a versatile strategy for the construction of fully synthetic and perfectly monodisperse non-viral gene delivery systems uniquely suited for optimization schemes.
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Multiply–linked cyclodextrin–aromatic hybrids: Caps, hinges and clips

TL;DR: A review article focuses specifically on aromatic modules in cage-type architectures, highlighting the intimate relationship between structure, supramolecular properties and performance in the target application.
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Dynamic Control of the Self-Assembling Properties of Cyclodextrins by the Interplay of Aromatic and Host-Guest Interactions.

TL;DR: Inclusion of adamantane carboxylate, a well-known βCD cavity-fitting guest, was found to either preserve the dimeric arrangement, leading to multicomponent species, or elicit dimer disruption.
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Xylylene Clips for the Topology-Guided Control of the Inclusion and Self-Assembling Properties of Cyclodextrins.

TL;DR: The topology of β-cyclodextrin can be molded, from toroidal to ovoid basket-shaped, by the installation of an o- or m-xylylene moiety connecting two consecutive d-glucopyranosyl units through the secondary O-2(I) and O-3(II) positions.
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Reversible Light-Induced Dimerization of Secondary Face Azobenzene-Functionalized β-Cyclodextrin Derivatives

TL;DR: In this article , an azobenzene moiety can be "clicked" to a single secondary O-2 position of β-cyclodextrin derivatives, affording 1,2,3-triazole-linked βCyD-azobenzenes derivatives that undergo reversible light controlled self-organization into dimers where the monomer components face their secondary rims.