Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions"
Skup podataka: uv-vis.zip, 1.39 MB Pravo pristupa: Otvoren pristup
Skup podataka: scxrd.zip, 358.89 KB Pravo pristupa: Otvoren pristup
Skup podataka: gc-ms.zip, 25.41 MB Pravo pristupa: Otvoren pristup
Skup podataka: hrms.zip, 962.5 KB Pravo pristupa: Otvoren pristup
Skup podataka: cd.zip, 2.51 MB Pravo pristupa: Otvoren pristup
Skup podataka: chiral-gc.zip, 188.16 KB Pravo pristupa: Otvoren pristup
Skup podataka: nmr.zip, 286.44 MB Pravo pristupa: Otvoren pristup
Prijavite se u repozitorij kako biste mogli spremiti objekt u svoju listu.
Citirajte ovaj rad
Kokan, Z. (2025). Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions" [Skup podataka]. doi:10.1039/D4DT02519A
Kokan, Zoran. Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions". Institut Ruđer Bošković, 2025. 18.12.2024. doi:10.1039/D4DT02519A
Kokan, Zoran. 2025. Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions". Institut Ruđer Bošković. doi:10.1039/D4DT02519A
Kokan, Z. 2025. Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions". Institut Ruđer Bošković. [Online]. [Citirano 18.12.2024.]. Preuzeto s: https://doi.org/10.1039/D4DT02519A
Kokan Z. Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions". [Internet]. Institut Ruđer Bošković: Zagreb, HR; 2025, [pristupljeno 18.12.2024.] Dostupno na: https://doi.org/10.1039/D4DT02519A
Z. Kokan, Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions", Institut Ruđer Bošković, 2025. Citirano: 18.12.2024. Dostupno na: https://doi.org/10.1039/D4DT02519A
Experimental data for "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions"
The experimental data for the research paper Bakija et al. "Supramolecular bidentate rhodium(i) or iridium(i) phosphine and oxazoline amino acid bioconjugates as selective catalysts for enantioselective reactions", Dalton Trans., 2025, Advance Article
Metodologija (engleski)
The original research data are given in their original format (which can be viewed by free downloadable software) or ASCI files for easier accessing and evaluating. ESI mass spectra were recorded on a HPLC-MS system (Agilent Technologies 1200) coupled with a 6410 Triple-Quadrupole mass spectrometer, operating in a positive ESI mode. High-resolution mass spectra were recorded on Agilent 6210 Time-of-Flight LC/MS (ESI). UV-Vis spectra were recorded on Cary 100 spectrophotometer and CD spectra were recorded on Jasco J-815 spectropolarimeter in 1.0 cm and 0.1 cm quartz Suprasil cells. Stock solutions of the isolated compounds were prepared for UV-Vis and CD measurements. The measured absorbance A (in UV-Vis) is converted to concentration-independent ε [M−1 cm−1] through the Lambert–Beer equation. The measured ellipticity θ [°] (in CD) is converted into the concentration independent Δε [M−1 cm−1] through the relation Δε = θ/(b × 32 982 × c), where b [cm] is the path length and c [M] is the concentration. NMR spectra were obtained on a Bruker Avance AV300 or AV600 spectrometer, operating at 300 or 600 MHz for 1H and 75 or 150 MHz for 13C; if not indicated further, the spectra were recorded at room temperature. Chemical shifts, δ (ppm), indicate a downfield shift from the internal standard, tetramethylsilane, TMS. Coupling constants, J, are given in Hz. Individual peaks are marked as: singlet (s), doublet (d), triplet (t), quartet (q), quintet (quin.) or multiplet (m). GC-MS data were recorded on Agilent 7890/5977 and Agilent 8860 GC/Agilent 5977 MSD with a SST EI 350 instruments and chiral GC data on Agilent 8890 GC instrument with a FID.
Šifra: KK.01.1.1.04.0013 Naziv (hrvatski): Inovativna rješenja u katalitičkim proizvodnim procesima za potrebe farmaceutske industrije Naziv (engleski): Innovative solutions in catalytic processes in the pharmaceutical industry Kratica: CAT PHARMA Voditelj: Srećko Kirin Pravna nadležnost: eu Financijer: Europska unija Linija financiranja: European Regional Development Fund
Projekt
Šifra: IP-2022-10-8456 Naziv (hrvatski): Supramolekulska asimetrična kataliza: Prijenos kiralnosti u koordinacijskim kavezima (Cage Cat) Naziv (engleski): Supramolecular asymmetric catalysis: Chirality transfer in coordination cages (Cage Cat) Kratica: Cage Cat Voditelj: Srećko Kirin Pravna nadležnost: Hrvatska Financijer: Hrvatska zaklada za znanost Linija financiranja: Research Projects