Phase Transformations And Dynamics Of 4-Cyano-4′-Pentylbiphenyl (5cb) By Nuclear Magnetic Resonance, Analysis Differential Scanning Calorimetry, And Wideangle X-Ray Diffraction Analysis

2002 ◽  
Vol 382 (1) ◽  
pp. 97-111 ◽  
Author(s):  
T. Mansaré ◽  
R. Decressain ◽  
C. Gors ◽  
V. K. Dolganov
1981 ◽  
Vol 46 (16) ◽  
pp. 3302-3305 ◽  
Author(s):  
Edmund J. Eisenbraun ◽  
Clinton E. Browne ◽  
Ernest L. Eliel ◽  
David L. Harris ◽  
Asadur Rahman ◽  
...  

2015 ◽  
Vol 2 (1) ◽  
pp. 13-20 ◽  
Author(s):  
Syed Nasir Abbas Bukhari ◽  
Ng Shin Hwei ◽  
Ibrahim Jantan

Current analytical techniques for characterizing solid-state pharmaceuticals include powder x-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, infrared spectroscopy, Raman spectroscopy, electron microscopy and nuclear magnetic resonance. Powder x-ray diffraction and differential scanning calorimetry are mainstream techniques but they lack spatial resolution. Scanning electron microscopy and micro-Raman spectroscopy provide good chemical and optical characterization but they are not capable of analysing very small nanoparticles. Transmission electron microscopy and nano-thermal analysis can provide explicit characterization of nanoparticles but they are invasive. Nuclear magnetic resonance offers good spatial resolution but its use is mainly limited by poor sensitivity and high costs. In view of the many challenges posed by existing methods, new and novel techniques are being continually researched and developed to cater to the growing number of solid formulations in the pipeline and in the market. Some of the recent advances attained in the solid-state analysis of pharmaceutical are summarized in this review article.


1994 ◽  
Vol 346 ◽  
Author(s):  
Walter G. Klemperer ◽  
Todd A. Marquart

ABSTRACTCentimeter-sized crystals of pyridine dodecasil 3C (all silica zeolite ZSM-39) have been prepared using hydrothermal seeded growth techniques and characterized by differential scanning calorimetry, nuclear magnetic resonance, optical microscopy and powder X-ray diffraction.


CrystEngComm ◽  
2018 ◽  
Vol 20 (22) ◽  
pp. 3105-3116 ◽  
Author(s):  
Roman Svoboda ◽  
Roman Bulánek ◽  
Dušan Galusek ◽  
Roghayeh Hadidimasouleh ◽  
Yadolah Ganjkhanlou

Differential scanning calorimetry and in situ X-ray diffraction analysis were used to study the products and mechanism of crystal formation in VOx–ZrO2 ceramics.


1988 ◽  
Vol 66 (6) ◽  
pp. 1467-1473 ◽  
Author(s):  
Carmen Avendaño ◽  
María Teresa Ramos ◽  
José Elguero ◽  
María Luisa Jimeno ◽  
Juana Bellanato ◽  
...  

Tautomerism of dibenzothiazolylmethane (1) and its C-methyl derivative (2) has been studied by 1H nuclear magnetic resonance, ultraviolet, and infrared spectroscopy using C,C-dimethyl (3) and N-methyl (4) derivatives as model compounds of the "CH" and "NH" forms, respectively. X-ray diffraction analysis of the "fixed" N-methyl derivative 4 shows that it corresponds to the Z-sE isomer 4b2. The CH tautomers are unstable in solution and they slowly isomerize into a mixture of NH tautomers that depends on the solvent and on the C-substituent (H or CH3).


Sign in / Sign up

Export Citation Format

Share Document