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Tin(II) cations stabilized by non-symmetric N,N',O-chelating ligands: synthesis and stability
Authors: Novák Miroslav | Turek Jan | Milasheuskaya Yaraslava | Syková Miriam | Dostál Libor | Stalmans Jesse | Růžičková Zdeňka | Jurkschat Klaus | Jambor Roman
Year: 2023
Type of publication: článek v odborném periodiku
Name of source: Dalton Transactions
Publisher name: Royal Society of Chemistry
Place: Cambridge
Page from-to: 2749-2761
Titles:
Language Name Abstract Keywords
cze Cínaté kationty stabilizované nesymetrickými N,N',O-chelatujícími ligandy: syntéza a stabilita V rámci této práce byla připravena série nových nesymetrických neutrálních N,N',O-chelatujících ligandů odvozených od a-iminopyridinu 2-(C(R1)=N(C6H3-2,6-iPr2))-6-(R2R3P=O)C5H3N (L1: R1 = H, R2 = R3 = Ph; L2: R1 = Me, R2 = R3 = Ph; L3: R1 = H; R2 = Ph, R3 = EtO; L4: R1 = Me, R2 = Ph, R3 = EtO; L5: R1 = H, R2 = R3 = iPrO; L6: R1 = Me, R2 = R3 = iPrO). Tyto ligandy byly následně studovány v reakcích se SnCl2 a Sn(OTf)2 s cílem studovat vliv různých funkčních skupin R2R3P=O na ionizaci SnCl2 a Sn(OTf)2. Zatímco všechny ligandy L1-6 poskytovaly odpovídající iontové cínaté komplexy [L1-6→SnCl]+[SnCl3]- (1 – 6), pouze ligandy L1, L4 a L6 byly schopny stabilizovat cínaté dikationty [ L1,4,6->Sn(H2O)][OTf]2 (7 – 9). Dále se ukázalo, že autoionizované sloučeniny [L3-6→SnCl]+[SnCl3]- obsahující ethylfenylfosfinátové a diisopropylfosfitové substituenty jsou nestabilní a podléhají eliminaci EtCl a iPrCl za vzniku nových sloučenin. Nakonec byly provedeny DFT studie pro lepší pochopení sterických a elektronických vlastností připravených sloučenin. cín; chelatující ligand; NMR; hemilabilita
eng Tin(II) cations stabilized by non-symmetric N,N',O-chelating ligands: synthesis and stability A series of novel non-symmetric neutral N,N',O-chelating ligands derived from the alpha-iminopyridine 2(C(R-1)=N(C6H3-2,6-iPr(2)))-6-((RRP)-R-2-P-3=O)C5H3N (L-1: R-1 = H, R-2 = R-3 = Ph; L-2: R-1 = Me, R-2 = R-3 = Ph; L-3: R-1 = H; R-2 = Ph, R-3 = EtO; L-4: R-1 = Me, R-2 = Ph, R-3 = EtO; L-5: R-1 = H, R-2 = R-3 = iPrO; L-6: R1 = Me, R-2 = R-3 = iPrO) were synthesized. Ligands L(1-6 )were reacted with SnCl2 and Sn(OTf)(2) with the aim of studying the influence of different (RRP)-R-2-P-3=O functional groups on the Lewis base mediated ionization of SnCl(2 )and Sn(OTf)(2). While all ligands L1-6 provided the corresponding ionic tin(II) complexes [L1-6 ->+ SnCl](+)[SnCl3](-) (1-6), only ligands L-1, L(4 )and L-6 were able to stabilize tin(II) dications [L-1,L-4,L-6-+ Sn(H2O)][OTf](2 )(7-9). The auto-ionized compounds [L3-6-+ SnCl](+)[SnCl3](-) possessing ethylphenyl phosphinate and diisopropylphosphite substituents undergo elimination of EtCl and iPrCl, respectively, yielding compounds 10-13. These can either be interpreted as neutral tin(II)phosphinate chloride (10, 11) and tin(II)phosphonate chloride (12, 13), respectively, containing Sn-O and Sn-Cl bonds, and a P=O -> SnCl2 interaction, or as zwitterionic compounds, where the positive charge of the central tin atom is compensated by an [OSnCl2]- anion. Finally, DFT studies were performed to better understand the steric and electronic properties of the ligands L(1-6 )as well as the nature of the bonds in the resulting products, with a particular focus on complexes 10-13. Tin; chelating ligands; NMR

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