Search results for "Proton NMR"
showing 10 items of 324 documents
Finely tuned nickel complexes as highly active catalysts affording branched polyethylene of high molecular weight: 1-(2,6-Dibenzhydryl-4- methoxyphen…
2018
Abstract A series of unsymmetrical 1,2-bis(imino)acenaphthenenickel(II) halides containing N-2,6-dibenzhydryl-4-methoxyphenyl – a single bulky group with adjusted electron donating properties – has been synthesized and characterized. These compounds adopt distorted tetrahedral geometry and their 1H NMR spectra show the paramagnetically shifted peaks. On activation with a low amount of Et2AlCl or ethylaluminum sesquichloride (EASC), these nickel complexes display high activity in ethylene polymerization, yielding the polyethylene of high molecular weight. They are also stable at elevated temperature; superb activity of 2.51 × 106 g of PE (mol of Ni)−1 h−1 can be attained at 90 °C. The result…
Polymerization of Triazolinediones withtrans-3,3-Dichloro-1-phenyl-1-propene
1997
The reaction of 4-phenyl-1,2,4-triazoline-3,5-dione (PhTD) (2) with trans-3,3-dichloro-1-phenyl-1-propene (4) was investigated at room and reflux temperatures in methylene chloride solution. Although the reaction is slow, it gives quantitative yield. This reaction leads to the formation of two 2:1 adducts via double Diels–Alder and Diels–Alder-Ene reactions in a ratio of about 1: 7. The major product was isolated by means of fractional crystallization as a pure compound and was characterized by infra-red (IR), 1H nuclear magnetic resonance (NMR), 13C NMR, mass spectra and elemental analysis. The structure of the minor product was determined by IR and 1H NMR. These compounds were used as mod…
Ring-opening polymerization of lactides using heterobimetallic yttrocene complexes
1999
Structurally characterized, chiral heterobimetallic yttrocene derivatives Li[Y(η 5 :η 1 -C 5 R 4 Si-Me 2 NCH 2 CH 2 OMe) 2 ] (R = Me, H) have been shown to be active in the controlled ring-opening polymerization of L-lactide to give poly(L-lactide)s with high molecular weights and moderately narrow molecular weight distributions (M w /M n < 1.50). Both transesterification and racemization appear to be less prominent. 'H NMR spectroscopic tetrad analysis of copolymers prepared using a mixture of L- and D-lactide demonstrates the absence of any preference for one enantiomer during the polymerization.
Influence of water, temperature and sucrose on dynamics in glassy starch-based products studied by low field 1H NMR
2009
Abstract In this study, the influence of both water content and temperature on the mobility of glassy starch-based matrices (starch alone or mixed with sucrose at the ratio 0% to 20% db) were studied using time domain 1 H NMR. The 2nd moment M 2 , and transversal relaxation time T 2 ∗ were used to study the molecular mobility of the rigid and mobile fraction of the NMR signal, respectively. The molecular mobility of the protons constituting the samples increased with water content (up to 13% wb) at all temperatures. For a given water content, both rigid and mobile protons exhibited a lower mobility in the presence of sucrose. When mobility characteristic parameters, M 2 second moment values…
Poly(Ethylene Glycol) Dimethacrylates with Cleavable Ketal Sites: Precursors for Cleavable PEG-Hydrogels.
2017
The authors introduce poly(ethylene glycol) (PEG) based macromonomers containing acid-labile ketal moieties as well as terminal methacrylate units that are amenable to radical polymerization. The synthesis of PEGs of different molecular weights (ranging from 2000 to 13 000 g mol-1 with polydispersities <1.15) with a central ketal unit (PEG-ketal-diol) and their conversion to PEG-ketal-dimethacrylates (PEG-ketal-DMA) is introduced. Degradation rates of both PEG-ketal-diols and PEG-ketal-DMA are investigated by in situ 1 H NMR kinetic studies in deuterated phosphate buffer. Hydrogels containing 0, 5, or 10 wt% of PEG-ketal-DMA and 100, 95, or 90 wt% of PEG-DMA, respectively, are synthesized a…
Novel meso-substituted porphyrins: Synthesis, characterization and photocatalytic activity of their TiO2-based composites
2009
Abstract Two series of novel meso-substituted porphyrins, namely 5,10,15,20-tetra[4-(3-phenoxy)-propoxy]phenyl porphyrin, the structural analogue 5,10,15,20-tetra[2-(3-phenoxy)-propoxy]phenyl porphyrin and their Co(II) Cu(II) and Zn(II) complexes were synthesized. The compounds were characterized using various spectroscopic techniques and their molecular structure was proposed based on density functional theory calculations. The diverse properties of the porphyrin derivatives result from the different stereochemistry of the particular substituents at the meso site on the macrocycle and are controlled also by the coordinated metal. The 1H NMR spectrum of the free-base porphyrin showed a comp…
Metal coordination of azurin in the unfolded state.
1998
Abstract1H NMR data applied to the paramagnetic cobalt(II) derivative of azurin from Pseudomonas aeruginosa have made it possible to show that the metal ion is bound to the protein in the unfolded state. The relaxation data as well as the low magnetic anisotropy of the metal ion indicate that the cobalt ion is tetrahedral in the unfolded form. The cobalt ligands have been identified as the residues Gly45, His46, Cys112 and His117. Met121 is not coordinated in the unfolded state. In this state, the metal ion is not constrained to adopt a bipyramidal geometry, as imposed by the protein when it is folded. This is clear confirmation of the rack-induced bonding mechanism previously proposed for …
NMR Study of Kraft Pulp Mill Waste and Natural Humic Substances
1988
High field proton NMR spectroscopy in DMSO-d6 solution is applied for structural analysis of main high molecular fractions of natural humus and waste lignin from kraft pulp mill. The spectra are similar in great part. Main differences appear in p-disubstituted benzene proton and -CH2 -CO-proton signals which are absent in spectrum of waste lignin obviously due to chlorination. A new observation of 51 Hz 1:1:1 triplet in both spectra is discussed.
How nitrogen modifies the nuclear magnetic shielding in tetraazanaphthalenes
2009
Although for planar conjugated hydrocarbons the out-of-plane component of proton magnetic shielding is an unquestionable quantitative aromaticity indicator, the same is not true for tetraazanaphthalenes. As in these compounds the (core + sigma)-currents associated to the nitrogen nuclei diminish the perpendicular component of shielding, abnormal values of (1)H NMR sigma(zz) are obtained. Therefore, a consistent aromaticity measure must be based only on the pi-contribution to the out-of-plane component of proton magnetic shielding. Otherwise, the behavior of these compounds in presence of an external magnetic field parallels that of naphthalene, with the nitrogen nuclei contributing to the r…
Synthesis of chlorinated alkylbibenzyls and 9-chlororetene
1995
Abstract The synthesis of chlorinated alkylbibenzyls and 9-chlororetene is described. These compounds were synthesized for use as model compounds in analytical and toxicological characterization. The structures of the synthesized model compounds found to be very similar to those identified in pulp mill effluent and products. The 1H NMR and mass spectral data for the compounds are also reported.