Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Guido, Orlandini"'
Autor:
Guido Orlandini
Publikováno v:
Pathos, Vol 30, Iss 4 (2023)
The pain threshold determines the extent of pain perception, and in some cases, its manifestation. Therefore, it is important in certain situations to increase the pain threshold. Measuring the pain threshold is challenging due to its approximate nat
Externí odkaz:
https://doaj.org/article/e789fabb025e4ce293ed7941e126564f
Autor:
Federica Cester Bonati, Margherita Bazzoni, Caterina Baccini, Valeria Zanichelli, Guido Orlandini, Arturo Arduini, Gianpiero Cera, Andrea Secchi
Publikováno v:
Molecules, Vol 28, Iss 2, p 595 (2023)
In this work, the ability of several bis-viologen axles to thread a series of heteroditopic tris(N-phenylureido)calix[6]arene wheels to give interwoven supramolecular complexes to the [3]pseudorotaxane type was studied. The unidirectionality of the t
Externí odkaz:
https://doaj.org/article/c3130ad169fb4cc8892706beba5ce9e5
Autor:
Serena Silvi, Margherita Bazzoni, Alberto Credi, Beatrice Cogliati, Marco Lucarini, Lorenzo Casimiro, Arturo Arduini, Andrea Secchi, Guido Orlandini
Publikováno v:
ORGANIC CHEMISTRY FRONTIERS 7 (2020): 648–659. doi:10.1039/c9qo01379b
info:cnr-pdr/source/autori:Orlandini, Guido; Casimiro, Lorenzo; Bazzoni, Margherita; Cogliati, Beatrice; Credi, Alberto; Lucarini, Marco; Silvi, Serena; Arduini, Arturo; Secchi, Andrea/titolo:Synthesis and properties of a redox-switchable calix[6]arene-based molecular lasso/doi:10.1039%2Fc9qo01379b/rivista:ORGANIC CHEMISTRY FRONTIERS/anno:2020/pagina_da:648/pagina_a:659/intervallo_pagine:648–659/volume:7
info:cnr-pdr/source/autori:Orlandini, Guido; Casimiro, Lorenzo; Bazzoni, Margherita; Cogliati, Beatrice; Credi, Alberto; Lucarini, Marco; Silvi, Serena; Arduini, Arturo; Secchi, Andrea/titolo:Synthesis and properties of a redox-switchable calix[6]arene-based molecular lasso/doi:10.1039%2Fc9qo01379b/rivista:ORGANIC CHEMISTRY FRONTIERS/anno:2020/pagina_da:648/pagina_a:659/intervallo_pagine:648–659/volume:7
The synthesis and characterisation of calix[6]arene-based lasso-like molecular structures is described. These interwoven structures consist of an electrochemical responsive N,N '-dialkylviologen arm covalently anchored at the upper rim of a triphenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85256cc9ada1db514e6ee527a8f747a6
https://doi.org/10.1039/c9qo01379b
https://doi.org/10.1039/c9qo01379b
Autor:
Guido Orlandini
Publikováno v:
Pathos, Vol 18, Iss 2-3, Pp 7-10 (2011)
Glia exerts a pathogenic role in the development and maintenance of pain. In the past, glia was considered only support material; the glia is 70 to 90 percent of the CNS cells. Normally in a resting state, it is activated by substances released from
Externí odkaz:
https://doaj.org/article/bcf7c138ea144e92ba226105a802be68
Autor:
Guido Orlandini
Publikováno v:
Pathos, Vol 18, Iss 1, Pp 9-13 (2011)
In some patients endometriosis causes persistent or chronic pain and is a specialistic algologic problem. Considering various possible pathogenic pain mechanisms, when pain therapy of endometriosis cannot be etiologic, far from be only symptomatic,
Externí odkaz:
https://doaj.org/article/703ef41895e741d3abf97e259f471ae4
Autor:
Guido Orlandini, Marco La Grua
Publikováno v:
Pathos, Vol 19, Iss 1-2 (2012)
In this review the knowledge about the mechanisms underlying the local anesthetics action, the validity of their efficacy, the relationship among the anesthetic effect duration, the doses used, the administration pathways - particularly those concern
Externí odkaz:
https://doaj.org/article/bb74460489e34adbb61a7d6443dfcb3f
Autor:
Guido Orlandini
Publikováno v:
Pathos, Vol 18, Iss 2-3 (2011)
Glia exerts a pathogenic role in the development and maintenance of pain. In the past, glia was considered only support material; the glia is 70 to 90 percent of the CNS cells. Normally in a resting state, it is activated by substances released from
Externí odkaz:
https://doaj.org/article/50c20821a2684aa5a3ce53b843c1e96a
Publikováno v:
Electrochimica Acta. 227:391-400
The development of functional materials and smart surfaces has received tremendous attention in recent years. The anchoring of molecular machines and the transfer of their properties on to solid substrates may facilitate the design of new smart devic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a31e6654096066945177b9f4e763532f
https://doi.org/10.1016/j.electacta.2016.12.169
https://doi.org/10.1016/j.electacta.2016.12.169
Autor:
Andrea Secchi, Arturo Arduini, Francesco Vita, Chiara Massera, Michela Vorti, Franco Ugozzoli, Valeria Zanichelli, Guido Orlandini
Publikováno v:
CrystEngComm. 18:5017-5027
A series of calix[4]arene semitubes (4a–c) having alkyl bridging spacers of different lengths and flexibilities on their lower rim was synthesised and characterised in solution and in the solid state by 1H NMR spectroscopy and X-ray crystallography
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6acf3f7a59787f26c6972d027c5c6409
https://doi.org/10.1039/c6ce00268d
https://doi.org/10.1039/c6ce00268d
Autor:
Margherita Venturi, Massimo Baroncini, Arturo Arduini, Giulio Ragazzon, Valeria Zanichelli, Lorenzo Degli Esposti, Guido Orlandini, Alberto Credi, Serena Silvi, Andrea Secchi
Publikováno v:
Orlandini, Guido ; Ragazzon, Giulio ; Zanichelli, Valeria ; Degli Esposti, Lorenzo ; Baroncini, Massimo ; Silvi, Serena ; Venturi, Margherita ; Credi, Alberto ; Secchi, Andrea ; Arduini, Arturo (2017) Plugging a bipyridinium axle into multichromophoric calix[6]arene wheels bearing naphthyl units at different rims. ChemistryOpen, 6 . pp. 64-72.
ChemistryOpen
ChemistryOpen
Tris‐(N‐phenylureido)‐calix[6]arene derivatives are heteroditopic non‐symmetric molecular hosts that can form pseudorotaxane complexes with 4,4′‐bipyridinium‐type guests. Owing to the unique structural features and recognition propertie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e43aab217a4a04963a4d78a7bda90f5
http://amsacta.unibo.it/5808/
http://amsacta.unibo.it/5808/
