A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
Dynamic Refolding of Ion-Pair Catalysts in Response to Different Anions (2019)


Neuvonen, A. J., Noutsias, D., Topić, F., Rissanen, K., Földes, T., Pápai, I., & Pihko, P. M. (2019). Dynamic Refolding of Ion-Pair Catalysts in Response to Different Anions. Journal of Organic Chemistry, 84(23), 15009-15019. https://doi.org/10.1021/acs.joc.9b01980


JYU-tekijät tai -toimittajat


Julkaisun tiedot

Julkaisun kaikki tekijät tai toimittajatNeuvonen, Antti J.; Noutsias, Dimitris; Topić, Filip; Rissanen, Kari; Földes, Tamás; Pápai, Imre; Pihko, Petri M.

Lehti tai sarjaJournal of Organic Chemistry

ISSN0022-3263

eISSN1520-6904

Julkaisuvuosi2019

Volyymi84

Lehden numero23

Artikkelin sivunumerot15009-15019

KustantajaAmerican Chemical Society

JulkaisumaaYhdysvallat (USA)

Julkaisun kielienglanti

DOIhttps://doi.org/10.1021/acs.joc.9b01980

Julkaisun avoin saatavuusEi avoin

Julkaisukanavan avoin saatavuus

Julkaisu on rinnakkaistallennettu (JYX)https://jyx.jyu.fi/handle/123456789/65607


Tiivistelmä

Four distinct folding patterns were identified in two foldamer-type urea-thiourea catalysts bearing a basic dimethylamino unit by a combination of X-ray crystallography, solution NMR studies, and computational studies (DFT). These patterns are characterized by different intramolecular hydrogen bonding schemes that arise largely from different thiourea conformers. The free base forms of the catalysts are characterized by folds where the intramolecular hydrogen bonds between the urea and the thiourea units remain intact. In contrast, the catalytically relevant salt forms of the catalyst, where the catalyst forms an ion pair with the substrate or substrate analogues, appear in two entirely different folding patterns. With larger anions that mimic the dialkyl malonate substrates, the catalysts maintain its native fold both in the solid state and in solution, but with smaller halide anions (fluoride, chloride and bromide), the catalysts fold around the halide anion (anion receptor fold) and the intramolecular hydrogen bonds are disrupted. Titration of catalyst hexafluoroacetylacetonate salt with tetra-n-butylammonium chloride results in dynamic refolding of the catalyst from the native fold to the anion receptor fold.


YSO-asiasanatanionitkatalyysikidetiederöntgenkristallografia

Vapaat asiasanatcatalysis; folding, anion binding; X-ray; solution structures; conformational change


Liittyvät organisaatiot

JYU-yksiköt:


Hankkeet, joissa julkaisu on tehty


OKM-raportointiKyllä

Raportointivuosi2019

JUFO-taso2


Viimeisin päivitys 2024-08-01 klo 21:39