A Zn(II) Metallocycle as Platform to Assemble a 1D + 1D → 1D Polyrotaxane via π···π Stacking of an Ancillary Ligand

Autor: Marzio Rancan, Giada Truccolo, Alice Carlotto, Silvio Quici, Lidia Armelao

Publikováno v: Inorganics, Vol 7, Iss 11, p 137 (2019)

A new [Zn2L2] metallocycle bearing two metal centers that can coordinate ancillary ligands and a pocket suitable to host guest molecules is reported. These two features are exploited by reacting the metallocycle with a pyridine ligand to self-assembl

Externí odkaz: https://doaj.org/article/82b978ec0ed04a36a18e8178fb99581e

Design and synthesis of new luminescent coordination networks of sql topology showing the highest degrees of interpenetration

Autor: Delia Blasi, Silvio Quici, Simonetta Orlandi, Pierluigi Mercandelli, Andrey V. Sokolov, Eugeny V. Alexandrov, Lucia Carlucci

Publikováno v: CrystEngComm. 24:5474-5486

The highest degree of interpenetration reported so far of 7- and 8-fold is realized in two luminescent sql 2D networks by self-assembly of a new nanometric-sized ligand with Ag(i) salts.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa54e9e63f6e844b72e462d7cb45c565
https://doi.org/10.1039/d2ce00884j

A Cu(ii) metallocycle for the reversible self-assembly of coordination-driven polyrotaxane-like architectures

Autor: Jacopo Tessarolo, Lidia Armelao, Giada Truccolo, Marzio Rancan, Zeno Tessari, Silvio Quici

Publikováno v: Dalton transactions (2003. Print) 47 (2018): 12079–12084. doi:10.1039/C8DT02693A
info:cnr-pdr/source/autori:Truccolo G.; Tessari Z.; Tessarolo J.; Quici S.; Armelao L.; Rancan M./titolo:A Cu(ii) metallocycle for the reversible self-assembly of coordination-driven polyrotaxane-like architectures/doi:10.1039%2FC8DT02693A/rivista:Dalton transactions (2003. Print)/anno:2018/pagina_da:12079/pagina_a:12084/intervallo_pagine:12079–12084/volume:47

We report the design and synthesis of a Cu(ii) metallocycle (1) and use the possibility to expand the Cu(ii) coordination sphere to self-assemble mechanically interlocked species via interpenetration. Metallocycle 1 can be used as a platform to rever

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73de4676833ad2aef59490ca24fb8d2e

Proton in a Confined Space: Structural Studies of H

Autor: Vijith, Kumar, Tullio, Pilati, Silvio, Quici, Michele R, Chierotti, Carlo, Nervi, Roberto, Gobetto, Giuseppe, Resnati

Publikováno v: Chemistry (Weinheim an der Bergstrasse, Germany). 23(58)

Experimental observations and modeling data are reported on the solid-state structural features of crypt- 111⋅HI (1) and the three-component co-crystals that 1 forms with α,ω-diiodoperfluoroalkanes 2 a-d. X-ray analyses indicate that, in all five

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dfa047eaeaa361749651bc786f4b0981
https://pubmed.ncbi.nlm.nih.gov/28657685

Solvent-control of photoinduced electron transfer via hydrogen bonding in a molecular triad made of a dinuclear chromophore subunit

Autor: Sebastiano Campagna, Antonino Arrigo, Francesco Nastasi, Giuseppina La Ganga, Fausto Puntoriero, Gabriella Zappalà, Antonino Licciardello, Silvio Quici, Marco Cavazzini

Publikováno v: Chemical physics letters
683 (2017): 96–104. doi:10.1016/j.cplett.2017.02.035
info:cnr-pdr/source/autori:Arrigo A.; Nastasi F.; La Ganga G.; Puntoriero F.; Zappala G.; Licciardello A.; Cavazzini M.; Quici S.; Campagna S./titolo:Solvent-control of photoinduced electron transfer via hydrogen bonding in a molecular triad made of a dinuclear chromophore subunit/doi:10.1016%2Fj.cplett.2017.02.035/rivista:Chemical physics letters (Print)/anno:2017/pagina_da:96/pagina_a:104/intervallo_pagine:96–104/volume:683

We have prepared a molecular triad containing a triphenylamine as the electron donor D subunit, an anthraquinone derivative as the acceptor A group, and a dinuclear Ru(II) species (P-P) based on terpyridine-like ligands as light-harvesting subunit, s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80a64ecb766a14e59595f3676509e0ed
http://hdl.handle.net/11570/3107825