Synthesis and properties of an Au6 cluster supported by a mixed N-heterocyclic carbene–thiolate ligand

2020 ◽  
Vol 56 (45) ◽  
pp. 6102-6105 ◽  
Author(s):  
Kirsi Salorinne ◽  
Renee W. Y. Man ◽  
Paul A. Lummis ◽  
Maryam Sabooni Asre Hazer ◽  
Sami Malola ◽  
...  
Keyword(s):  

The preparation of a novel Au6 cluster bearing a bidentate mixed carbene–thiolate ligand is presented.


Nanomaterials ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 46
Author(s):  
Jae Hyun Kim ◽  
Joohoon Kim

Here, we report a post-synthesis functionalization of the shell of Au nanoclusters (NCs) synthesized using glutathione as a thiolate ligand. The as-synthesized Au NCs are subjected to the post-synthesis functionalization via amidic coupling of dopamine on the cluster shell to tailor photoluminescence (PL) and electrochemiluminescence (ECL) features of the Au NCs. Because the NCs’ PL at ca. 610 nm is primarily ascribed to the Au(I)-thiolate (SG) motifs on the cluster shell of the NCs, the post-synthesis functionalization of the cluster shell enhanced the PL intensity of the Au NCs via rigidification of the cluster shell. In contrast to the PL enhancement, the post-synthesis modification of the cluster shell does not enhance the near-infrared (NIR) ECL of the NCs because the NIR ECL at ca. 800 nm is ascribed to the Au(0)-SG motifs in the metallic core of the NCs.



2004 ◽  
Vol 43 (17) ◽  
pp. 2290-2293 ◽  
Author(s):  
Yasuhiro Ohki ◽  
Hitomi Sadohara ◽  
Yuko Takikawa ◽  
Kazuyuki Tatsumi


2014 ◽  
Vol 136 (49) ◽  
pp. 17016-17023 ◽  
Author(s):  
Praneeth Reddy Nimmala ◽  
Amala Dass
Keyword(s):  


2015 ◽  
Vol 71 (10) ◽  
pp. m181-m182
Author(s):  
Peter W. R. Corfield ◽  
Mary Bailey

The title compound, [Au(C18H10F4PS)Cl2], crystallizes as neutral molecules, with the AuIIIatom coordinated by two Cl atoms and by the P and S atoms of the bidentate phosphanyl thiolate ligand, in a slightly distorted square-planar environment. The molecules are linked into centrosymmetric dimersvialong axial Au—Cl bonds of 3.393 (4) Å. This axial Au—Cl distance is longer than is usually seen, although one other example has been given. Dimer formation may explain the unexpectedly low solubility of the compound in common polar solvents. There is also a separate intermolecular Au—F contact of 3.561 (6) Å, but this distance seems too long to be regarded as a bond. Two putative C—H...F hydrogen bonds appear to link the dimers into sheets parallel to (110). There is a short intermolecular F...F contact of 2.695 (10) Å between two dimers related by the twofold axis.



1992 ◽  
Vol 47 (5) ◽  
pp. 645-655 ◽  
Author(s):  
D. Sellmann ◽  
H. Schillinger ◽  
F. Knoch

Ni(II) salts and the tetradentate thioether-thiolate ligand ′S4-C2′2- (= 1,2-bis(2-mercaptophenylthio)ethane(2-)) yield [Ni(′S4-C2′)]x (1), that also forms when Na2[Ni(′S2′ )2] (′S22-′ = o-benzenedithiolate(2-)) is alkylated by 1,2-dibromoethane. In boiling pyridine 1 adds two solvent molecules and gives pseudooctahedral [Ni(pyr)2(′S4-C2′ )] (2) which was characterized by X-ray structure determination. Reaction of 1 with PMe3 yields [Ni(PMe3)(′S4-C2′)] (4). X-ray structure determination of 4 showed that the Ni center is surrounded by one P and four S atoms in a distorted tetragonal pyramid in which the P atom, one thioether S atom and both of the thiolate S atoms form the base while the second thioether S atom occupies the apical position. Reaction of 1 with n-BuLi leads to removal of the C2H4 bridge of the ′S4-C2′2- ligand and formation of Li2[Ni(′S2′)2].When [Ni(acac)2]3 is reacted with ′buS4-C2′2 (= 1,2-bis(3,5-ditertiarybutyl-2-mercaptophenylthio)ethane(2-)) which is analogous to ′S4-C2′2-, the trinuclear [Ni(′buS4-C2′)]3 (3) forms. 3 · THF was characterized by X-ray structure determination. It contains one tetrahedrally distorted and two planar [NiS4] cores that are connected via the C2H4 groups of the ligands such that a macrocycle forms. PMe3 cleaves 3 to give mononuclear [Ni(PMe3)(′buS4-C2′)] (5). Due to its lability, it was characterized only by spectroscopic methods.



1997 ◽  
Vol 36 (27) ◽  
pp. 6454-6456 ◽  
Author(s):  
M. Mar Artigas ◽  
Olga Crespo ◽  
M. Concepción Gimeno ◽  
Peter G. Jones ◽  
Antonio Laguna ◽  
...  


2014 ◽  
Vol 136 (45) ◽  
pp. 15865-15868 ◽  
Author(s):  
Lina G. AbdulHalim ◽  
Nuwan Kothalawala ◽  
Lutfan Sinatra ◽  
Amala Dass ◽  
Osman M. Bakr


1993 ◽  
Vol 115 (4) ◽  
pp. 1413-1421 ◽  
Author(s):  
Julea N. Butt ◽  
Artur Sucheta ◽  
Fraser A. Armstrong ◽  
Jacques Breton ◽  
Andrew J. Thomson ◽  
...  


Sign in / Sign up

Export Citation Format

Share Document