Phosphinohydrazines. Part IV. Coordination compounds of N,N-dimethyl,N′-diphenylphosphinohydrazine and N,N-dimethyl-N′-diphenylthiophosphinatohydrazine

1970 ◽  
Vol 48 (3) ◽  
pp. 401-404 ◽  
Author(s):  
E. W. Ainscough ◽  
L. K. Peterson ◽  
D. E. Sabourin
Keyword(s):  
Molecular Weight ◽  
Nuclear Magnetic Resonance ◽  
Coordination Compounds ◽  
Donor Site ◽  
Membered Ring ◽  
Monomeric Form ◽  
Coordinate Structure ◽  
Polar Solvents ◽  
Uncertain Structure ◽  
Ring Structures

A study of complexes of (a) N,N-dimethyl,N′-diphenylphosphinohydrazine, DPH, viz., Pd(DPH)Cl2, Pd(DPH)2Cl2, [Pd(DPH)2Cl]ClO4, Pt(DPH)2Cl2, Pt(DPH)Cl4, Hg(DPH)Cl2; (b) N,N-dimethyl,N´-diphenylthiophosphinatohydrazine, DPS, viz., Pd(DPS)Cl2, Pt(DPS)Cl4, Ag(DPS)NO3, Zn(DPS)Cl2, Cd(DPS)Cl2, and Hg(DPS)Cl2, and (c) N,N-dimethylhydrazine, DMH, viz., Zn(DMH)2Cl2 and Cd(DMH)Cl2, has been carried out using conductivity, molecular weight, infrared, and nuclear magnetic resonance measurements. DPH functions mostly as a unidentate ligand, with the phosphorus atom as the preferred donor site. Thus Pd(DPH)Cl2 is a chlorobridged dimer in solution in weakly polar solvents, while the monomeric form in polar solvents is of uncertain structure. A trans, four-coordinate structure is consistent for Pd(DPH)2Cl2. For [Pd(DPH)2Cl]ClO4, however, one DPH ligand is chelating through the phosphorus and terminal nitrogen atoms, while the second ligand is unidentate; the compound is a monomeric uni–univalent electrolyte in nitrobenzene. The ligand DPS appears to chelate via the sulfur and central nitrogen atoms, giving four-membered ring structures; a cis configuration is suggested for Pd(DPS)Cl2. Zn(DMH)2Cl2 is monomeric in solution, with the Me2N group coordinated to the metal.

Study on Structure and Tanning Properties of Copolymer of Resorcinol and 3,5-Dihydroxyl Benzoic Acid

2012 ◽  
Vol 487 ◽  
pp. 48-52
Author(s):  
Sheng Hua Lv ◽  
Gong Rui ◽  
Di Li
Keyword(s):  
Molecular Weight ◽  
Nuclear Magnetic Resonance ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Gel Permeation Chromatography ◽  
Radical Copolymerization ◽  
Mass Ratio ◽  
Monomer Composition ◽  
Chrome Tanning ◽  
Gel Permeation

The radical copolymerization of resorcinol (RSC) and 3,5-dihydroxyl benzoic (DHBA) was carried out in water by the initiator of horseradish (HRP)/H2O2. It was discussed that the effects of monomer composition on the properties of the copolymer. The best monomer mass ratio of RSC:DHBA was 60:40 and the shrink temperature can reached to 88.5oC. The tanning result indicated that the copolymer of RSC and DHPA has particularly excellent tanning properties and can be served as leather tannage substitute for chrome tanning materials. And also the mechanism of the HRP initiated copolymerization was proposed. The structure and molecular weight of the copolymer was characterized by Fourier Transform Infrared spectroscopy (FTIR), Nuclear Magnetic Resonance (NMR) and Gel Permeation Chromatography (GPC). The copolymer can be as tannage and retannage in making leather process. The results showed that it has excellent tanning properties and retanning effects.

scholarly journals Cleavage of the Graft Bonds in PVDF–g–St Films by Boiling Xylene Extraction and the Determination of the Molecular Weight of the Graft Chains

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1098 ◽  
Author(s):  
Chen ◽  
Seko
Keyword(s):  
Molecular Weight ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Thermal Degradation ◽  
Gel Permeation Chromatography ◽  
Extraction Time ◽  
Gel Permeation ◽  
Irradiation Graft ◽  
Nuclear Magnetic

To determine the molecular weight of graft chains in grafted films, the polystyrene graft chains of PVDF–g–St films synthesized by a pre-irradiation graft method are cleaved and separated by boiling xylene extraction. The analysis of the extracted material and the residual films by FTIR, nuclear magnetic resonance (NMR), and gel permeation chromatography (GPC) analyses indicates that most graft chains are removed from the PVDF–g–St films within 72 h of extraction time. Furthermore, the molecular weight of the residual films decreases quickly within 8 h of extraction and then remains virtually unchanged up to 72 h after extraction time. The degradation is due to the cleavage of graft bonds, which is mainly driven by the thermal degradation and the swelling of graft chains in solution. This allows determination of the molecular weight of graft chains by GPC analysis of the extracted material. The results indicate that the PVDF–g–St prepared in this study has the structure where one or two graft chains hang from each PVDF backbone.

Predicting skin permeation rate from nuclear magnetic resonance spectra

2016 ◽  
Vol 18 (16) ◽  
pp. 4468-4474 ◽  
Author(s):  
Nan An ◽  
John-Hanson Machado ◽  
Yuechuan Tang ◽  
Jakub Kostal ◽  
Adelina Voutchkova-Kostal
Keyword(s):  
Molecular Weight ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Spectroscopic Data ◽  
Chemical Structure ◽  
Skin Permeation ◽  
Permeation Rate ◽  
Organic Chemicals ◽  
Predictive Method ◽  
Nuclear Magnetic Resonance Spectra

A predictive method is reported for estimating skin permeation of organic chemicals exclusively from NMR spectroscopic data and molecular weight, which does not require knowledge of chemical structure.

Structural studies of the capsular polysaccharide from Haemophilus pleuropneumoniae serotype 2

1987 ◽  
Vol 65 (5) ◽  
pp. 414-422 ◽  
Author(s):  
Eleonora Altman ◽  
Jean-Robert Brisson ◽  
Malcolm B. Perry
Keyword(s):  
Molecular Weight ◽  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
High Molecular Weight ◽  
Capsular Polysaccharide ◽  
Structural Studies ◽  
High Molecular Weight Polymer ◽  
Molecular Weight Polymer ◽  
Structure Formula ◽  
Nuclear Magnetic

The capsular polysaccharide of Haemophilus pleuropneumoniae serotype 2 (ATCC 27089) is composed of D-glucose (two parts), D-galactose (one part), glycerol (one part), and phosphate (one part). Hydrolysis, dephosphorylation, methylation, enzymic studies, and 1H and 13C nuclear magnetic resonance experiments showed that the polysaccharide is a high molecular weight polymer of a tetrasaccharide repeating units, linked by monophosphate diester and having the following structure:[Formula: see text]

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