Tetrathiafulvalene - a redox-switchable building block to control motion in mechanically interlocked molecules. [PDF]
Beilstein J Org Chem, 2018 With the rise of artificial molecular machines, control of motion on the nanoscale has become a major contemporary research challenge. Tetrathiafulvalenes (TTFs) are one of the most versatile and widely used molecular redox switches to generate and ...
Schröder HV, Schalley CA.
europepmc +3 more sources
X-Ray Crystallographic Data on Certain Substituted 1,2- and 1,3-Dithiolium Salts, and two Substituted 1,2-Dithioles. [PDF]
Acta Chemica Scandinavica, 1963 Asbjørn Hordvik +4 more
openaire +2 more sources
Iminium Salts of ω-Dithiafulvenylpolyenals: An Easy Entry to the Corresponding Aldehydes and Doubly Proaromatic Nonlinear Optic-phores [PDF]
, 2008 A short, high-yielding route to ω-dithiafulvenylpolyenals (1) via the corresponding iminium salts (2) and starting from trimethyl-1,3-dithiolium tetrafluoroborate is reported.
B. Villacampa +11 more
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Tris(pentafluorophenyl)borane and beyond: modern advances in borylation chemistry [PDF]
, 2017 As main-group chemistry, in particular boron chemistry, has expanded and developed over the past 20 years, one reagent has risen to prominence as well.
James R. Lawson +3 more
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Novel 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives bridged by a crown ether unit at the 1,8-positions: A new type of redox-switchable hosts undergoing reversible structural changes [PDF]
, 2006 Novel redox-switchable host molecules (2) composed of a 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene unit and a crown ether moiety bridging the 1,8-positions have been synthesized.
Fujimori, K +3 more
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A binaphthol-substituted tetrathiafulvalene with axial chirality and its enantiopure TCNQF4 charge-transfer salts [PDF]
, 2011 International audienceA chiral tetrathiafulvalene (1) bearing a binaphtholdimethylene moiety on one side, an ethylenedithio substituent on the other side, is prepared from atropoisomeric (R)-, (S)- and racemic (R,S)-binaphthol. Its oxidation potential (0.
Fourmigué, Marc +2 more
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Functionalised tetrathiafulvalene- (TTF-) macrocycles: recent trends in applied supramolecular chemistry [PDF]
, 2018 Tetrathiafulvalene (TTF) has been extensively explored as a π-electron donor in supramolecular systems. Over the last two decades substantial advances have been made in terms of constructing elaborate architectures based on TTF and in exploiting the ...
A. Jana +7 more
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Metallkomplexe mit biologisch wichtigen Liganden, LXV [PDF]
, 1993 Cp*Co(CO)I2 (Cp* = 5-C5Me5), [(6-arene)RuCl2]2 (arene = p-cymene, hexamethylbenzene), and [Cp*MCl2]2 (M = Rh, Ir) react with -amino amides and various peptide esters to give the N,O-chelate complexes [Cp*(I)Co - NH2C(H)(R1)C(NHR2)-O]+ (1), [(6-arene ...
Beck +32 more
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Glycine Residue Twists HOMO¿HOMO Interactions in a Molecular Conductor [PDF]
, 2022 We report on radical cation salts of EDT-TTF cores bearing a glycine residue with hydrogenosulfate, [HSO4−], or the amphoteric para- carboxybenzenesulfonate, [HO2C-C6H4-SO3−].
Alemany i Cahner, Pere +7 more
core +1 more source
Studies in the dithiole series [PDF]
, 1963 Using previously developed methods, several new dithiolium salts have been prepared, and others have been synthesised by modification of Known methods. 3-Benzyl-5-phenyl-I,2-ditniolium perchlorate has been prepared by reaction of benzoylphenylacetone
McKinnon, David Mackie
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