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Structural Evidence for Pnictogen-Centered Lewis Acidity in Cationic Platinum-Stibine Complexes Featuring Pendent Amino or Ammonium Groups.


ABSTRACT: As part of our continuing interest in the chemistry of cationic antimony Lewis acids as ligands for late transition metals, we have now investigated the synthesis of platinum complexes featuring a triarylstibine ligand substituted by an o-[(dimethylamino)methyl]phenyl group referred to as ArN. More specifically, we describe the synthesis of the amino stibine ligand Ph2SbArN (L) and its platinum dichloride complex [LPtCl]Cl which exists as a chloride salt and which shows weak coordination of the amino group to the antimony center. We also report the conversion of [LPtCl]Cl into a tricationic complex [LHPt(SMe2)]3+ which has been isolated as a tris-triflate salt after reaction of [LPtCl]Cl with SMe2, HOTf and AgOTf. Finally, we show that [LHPt(SMe2)][OTf]3 acts as a catalyst for the cyclization of 2-allyl-2-(2-propynyl)malonate.

SUBMITTER: Rodrigues RR 

PROVIDER: S-EPMC8036533 | biostudies-literature | 2021 Apr

REPOSITORIES: biostudies-literature

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Structural Evidence for Pnictogen-Centered Lewis Acidity in Cationic Platinum-Stibine Complexes Featuring Pendent Amino or Ammonium Groups.

Rodrigues Roberta R RR   Gabbaï François P FP  

Molecules (Basel, Switzerland) 20210401 7


As part of our continuing interest in the chemistry of cationic antimony Lewis acids as ligands for late transition metals, we have now investigated the synthesis of platinum complexes featuring a triarylstibine ligand substituted by an <i>o</i>-[(dimethylamino)methyl]phenyl group referred to as Ar<sup>N</sup>. More specifically, we describe the synthesis of the amino stibine ligand Ph<sub>2</sub>SbAr<sup>N</sup> (<b>L</b>) and its platinum dichloride complex [<b>L</b>PtCl]Cl which exists as a c  ...[more]

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