Publikace detail

Exploring Differences between Bis(aldimino)- and amino-aldimino-N,C,N-Pincer-Stabilized Pnictinidenes: Limits of Synthesis, Structure, and Reversible Tautomerization-Controlled Oxidation

Rok: 2022

Druh publikace: článek v odborném periodiku

Název zdroje: Organometallics

Název nakladatele: American Chemical Society

Místo vydání: Washington

Strana od-do: 2535-2550

Tituly:

Jazyk	Název	Abstrakt	Klíčová slova
cze	Výzkum rozdílů mezi bis(aldimino)- a amino-aldimino-N,C,N-Pincer-Stabilizovaných pniktinidenů: Limity syntézy, struktury a vratné oxidace	Dva typa N,C,N-chelatovaných pniktinidenů, [2-(RNHCH2)-6-(RNHCH2)-6-(RN = CH)C6H3]E (1-E-R) a [2,6-(RN=CH)(2)C6H3]E (2-E-R, E = As, Sb, Bi), byly připraveny pro tuto studii. Déle byly zkoumány jejich reakce s K-selektridem nebo KC8.	bis(aldimino)-N,C,N-Pincer; pniktinideny; komplexy; reaktivita; sb; amino-aldimino-N,C,N-Pincer; bi
eng	Exploring Differences between Bis(aldimino)- and amino-aldimino-N,C,N-Pincer-Stabilized Pnictinidenes: Limits of Synthesis, Structure, and Reversible Tautomerization-Controlled Oxidation	Two types of N,C,N-chelated pnictinidenes, i.e., [2-(RNHCH2)-6-(RNHCH2)-6-(RN = CH)C6H3]E (1-E-R) and [2,6-(RN=CH)(2)C6H3]E (2-E-R, where E = As, Sb, Bi), are targeted in this study. 2-E-R could be obtained by simple reduction of respective precursors [2,6-(RN=CH)(2)C6H3]ECl2 (i.e., (2-E-R)Cl-2) with KC8 for E = As, Sb, or Bi with R being iBu, Ad, or Dipp. By contrast, the utilization of a bulky hydride, i.e., K-selectride, allowed the isolation of 1-E-R for E = As or Sb and R = Dipp, while the utilization of other pincer ligands, where R = tBu or Ad, led only to mixtures of both 1-E-R and 2-E-R. For bismuth, even the Dipp-substituted pincer ligand provided a mixture of 1-Bi-Dipp and 2-Bi-Dipp only. The structures and chemical properties of these sets of compounds, i.e., 1-E-Dipp, 2-E-tBu, and 2-E-Dipp, were compared using X-ray diffraction analysis, UV-vis spectroscopy including an extensive theoretical study, and CV measurements. The oxidation of 2-E-Dipp (E = As, Sb, Bi) by air resulted only in the formation of complicated mixtures, while oxidation of 1-E-Dipp (E = As or Sb) cleanly produces (1'-E-Dipp)OH as a result of a tautomeric NH -> OH shift at elusive oxides (1-E-Dipp)O under formation of a new E-N covalent bond. To examine the potential of such tautomerization-driven stabilization of oxidation products, the reactivity of 1-E-Dipp (E = As or Sb) toward other chalcogens is also reported, including a theoretical study.	ncn-chelated organoantimony(iii); bond covalent radii; n,c,n-chelated antimony(iii); phosphinidene-transfer; crystal-structures; complexes; sb; reactivity; chemistry; bi

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