A FRET-based ratiometric fluorescent probe to detect cysteine – The cells imaging were used by Leica TCS SP8 confocal microscope. Figure S1. 1H NMR spectrum of CP-K in DMSO-d6. Figure S4. The UV-vis spectra of probe CP-K (10.0 µM) in the presence of NaHSO3 (0–10.
2g1: 1H NMR (500 MHz, DMSO-d6) δ 9.95 (s, 1H), 9.57 (s, 1H), 7.91 (d, J = 8.7 Hz, 2H), 7.65-7.42 (m, 2H). 13C NMR (126 MHz, DMSO-d6) δ 198.98, 138.45,
These 1H NMR data correspond to the bis-methoxy adduct of 2a.
(96% yield). 1H NMR (δ, 23 °C, DMSO-d6): 8.03 (s, 1H, OH proton exchangeable with D2O),
(total yield: 6.9%) 1H-NMR of potassium 4,4′-(benzo[b]phenazine-6,11.
(a) Concentration-dependent absorption spectra of DAT-4COOH/MEEA (1:4) in DMSO at room temperature. (b) The absorbance of.
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1H DPFGSE NOE (500 MHz, d6-acetone, mix = 300 ms, d1 = 10 s). OTBS. OTBS. H. H. O. H. O. H. Ph3CO. NO2. O. OTBS. TBSO. O. OCPh3. O2N. ≡.
(6): 1H NMR spectrum of cyanoacetanilide (1d.
tert-butyl alcohol and dimethyl sulfoxide (DMSO). Deoxycholic acid was added to the dye solution as a coadsorbent at a concentration of 20 mM. 0.2 mM.
May 17, 2019.
in DMSO-d6, H is strongly coordinated (H-bonded) by DMSO oxygen atoms, resulting in substantial shielding. The chemical shift is ≈3.33 ppm.
This data set contains the qHNMR spectrum of Liquiritigenin acquired at 400 MHz in DMSO-d6. The sample was prepared with 3,5-dinotrobenzoic acid as.
Subsequently, a fresh solution of 10 mg of FITC in 10 mL of dry dimethylsulfoxide (DMSO, Sigma-Aldrich.
in de-ionized water in 37 °C for 1 h at a concentration of 5.0 w/v%.
Perkin Elmer 20 analyzer was utilized for elemental analysis of all compounds. 1H NMR and 13C NMR spectra were run on JEOL 400 MHz and Bruker Avance III 400 MHz using residual solvent as the internal.
Nov 11, 2015.
Fig 2. 1H NMR spectra of gallic acid (top) and gallic acid + DPPH radical (bottom) in DMSO-d6.
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1H and 13C NMR spectra of ICZs 4a-j. S12. 3. 1H and 13C NMR spectra of ICZs 5a-j. S13. 4.
Page S2. ©ARKAT USA, Inc. 1H NMR (solvent: DMSO-d6).
Test of the uranium adsorption selectivity of the hydrogel.
Table S1. 1H NMR Data2 proton mult. THF-d 8. CD2Cl2. CDCl3 toluene-d 8. C6D6.
dimethyl sulfoxide. CH3.
H NMR data by chemical shift in ppm) shift.
The synthesis and biological evaluation of sanguinarine derivatives as – Technologies); detector: PDA-100 photodiode array; inJector: ASI-100 autoinJector; pump: p-680A). A flow rate of 1.0 mL/min was used with mobile phase of MeOH in H2O. 361.8 mmol, 2.89 eq) and K2CO3.
Figure S16 shows 1H NMR spectrum of HepMAm. The peaks at 5.69 and 5.44 ppm.
A certain mass of the monomer NASC was dissolved in a mixed solvent of DMSO and water (7/3, v/v) according to the desired.