<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(2)</volume><submitter>Silva RAL</submitter><pubmed_abstract>Gold and nickel bisdithiolene complexes with methyl and tert-butyl substituted thiophenetetrathiafulavalenedithiolate ligands (?-mtdt and ?-tbtdt) were prepared and characterized. These complexes were obtained, under anaerobic conditions, as tetrabutylammonium salts. The diamagnetic gold monoanion (n-Bu?N)[Au(?-mtdt)?] (3) and nickel dianionic species (n-Bu?N)x[Ni(?-mtdt)?] (x = 1,2) (4) were similar to the related non-substituted extended thiophenic-TTF (TTF = tetrathiafulvalene) bisdithiolenes. However the introduction of the large, bulky substituent tert-butyl, led to the formation of a Au (I) dinuclear complex, (n-Bu?N)?[Au?(?-tbtdt)?] (5). The neutral methyl substituted gold and nickel complexes were easily obtained through air or iodine exposure as polycrystalline or amorphous fine powder. [Au(?-mtdt)?] (6) and [Ni(?-mtdt)?] (7) polycrystalline samples display properties of a metallic system with a room temperature electrical conductivity of 0.32 S/cm and ?4 S/cm and a thermoelectric power of ?5 µV/K and ?32 µV/K, respectively. While [Au(?-mtdt)?] (6) presented a Pauli-like magnetic susceptibility typical of conducting systems, in [Ni(?-mtdt)?] (7) large magnetic susceptibilities indicative of high spin states were observed. Both electric transport properties and magnetic properties for gold and nickel [M(?-mtdt)?] are indicative that these compounds are single component molecular conductors.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6017561</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Gold and Nickel Extended Thiophenic-TTF Bisdithiolene Complexes.</pubmed_title><pmcid>PMC6017561</pmcid><pubmed_authors>Silva RAL</pubmed_authors><pubmed_authors>Vieira BJC</pubmed_authors><pubmed_authors>Santos IC</pubmed_authors><pubmed_authors>Rabaca S</pubmed_authors><pubmed_authors>Coutinho JT</pubmed_authors><pubmed_authors>Andrade MM</pubmed_authors><pubmed_authors>Almeida M</pubmed_authors><pubmed_authors>Belo D</pubmed_authors><pubmed_authors>Lopes EB</pubmed_authors><pubmed_authors>Pereira LCJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Gold and Nickel Extended Thiophenic-TTF Bisdithiolene Complexes.</name><description>Gold and nickel bisdithiolene complexes with methyl and tert-butyl substituted thiophenetetrathiafulavalenedithiolate ligands (?-mtdt and ?-tbtdt) were prepared and characterized. These complexes were obtained, under anaerobic conditions, as tetrabutylammonium salts. The diamagnetic gold monoanion (n-Bu?N)[Au(?-mtdt)?] (3) and nickel dianionic species (n-Bu?N)x[Ni(?-mtdt)?] (x = 1,2) (4) were similar to the related non-substituted extended thiophenic-TTF (TTF = tetrathiafulvalene) bisdithiolenes. However the introduction of the large, bulky substituent tert-butyl, led to the formation of a Au (I) dinuclear complex, (n-Bu?N)?[Au?(?-tbtdt)?] (5). The neutral methyl substituted gold and nickel complexes were easily obtained through air or iodine exposure as polycrystalline or amorphous fine powder. [Au(?-mtdt)?] (6) and [Ni(?-mtdt)?] (7) polycrystalline samples display properties of a metallic system with a room temperature electrical conductivity of 0.32 S/cm and ?4 S/cm and a thermoelectric power of ?5 µV/K and ?32 µV/K, respectively. While [Au(?-mtdt)?] (6) presented a Pauli-like magnetic susceptibility typical of conducting systems, in [Ni(?-mtdt)?] (7) large magnetic susceptibilities indicative of high spin states were observed. Both electric transport properties and magnetic properties for gold and nickel [M(?-mtdt)?] are indicative that these compounds are single component molecular conductors.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Feb</publication><modification>2021-02-21T12:10:53Z</modification><creation>2019-03-27T00:06:37Z</creation></dates><accession>S-EPMC6017561</accession><cross_references><pubmed>29443956</pubmed><doi>10.3390/molecules23020424</doi></cross_references></HashMap>