Recognition of dicarboxylic acids by 3,3′-bipyridine amide based receptors and its supramolecular behavior in solid state

CrystEngComm ◽  
2008 ◽  
Vol 10 (5) ◽  
pp. 507 ◽  
Author(s):  
Shyamaprosad Goswami ◽  
Subrata Jana ◽  
Hoong-Kun Fun
Keyword(s):  
Solid State ◽  
Dicarboxylic Acids

Ionic Solid-State Dimers and Polymers Derived from Imidazolium Dicarboxylic Acids

2006 ◽  
Vol 12 (15) ◽  
pp. 4014-4020 ◽  
Author(s):  
Zhaofu Fei ◽  
Wee Han Ang ◽  
Tilmann J. Geldbach ◽  
Rosario Scopelliti ◽  
Paul J. Dyson
Keyword(s):  
Solid State ◽  
Dicarboxylic Acids ◽  
Ionic Solid

Solid-State Chlorodecarboxylation of Mono- and Dicarboxylic Acids with the Pb(OAc)4—MCl System.

ChemInform ◽  
2005 ◽  
Vol 36 (33) ◽  
Author(s):  
G. I. Nikishin ◽  
L. L. Sokova ◽  
A. O. Chizhov ◽  
V. D. Makhaev ◽  
N. I. Kapustina
Keyword(s):  
Solid State ◽  
Dicarboxylic Acids

Solid-state NMR studies of theophylline co-crystals with dicarboxylic acids

2014 ◽  
Vol 100 ◽  
pp. 322-328 ◽  
Author(s):  
Edyta Pindelska ◽  
Agnieszka Sokal ◽  
Lukasz Szeleszczuk ◽  
Dariusz Maciej Pisklak ◽  
Waclaw Kolodziejski
Keyword(s):  
Solid State ◽  
Solid State Nmr ◽  
Dicarboxylic Acids ◽  
Nmr Studies

Polymorphic and Isomorphic Cocrystals of a N-Salicylidene-3-aminopyridine with Dicarboxylic Acids: Tuning of Solid-State Photo- and Thermochromism

2016 ◽  
Vol 120 (18) ◽  
pp. 10001-10008 ◽  
Author(s):  
Andrea Carletta ◽  
Xavier Buol ◽  
Tom Leyssens ◽  
Benoît Champagne ◽  
Johan Wouters
Keyword(s):  
Solid State ◽  
Dicarboxylic Acids

Dynamic Molecular Recognition in Solid State for Separating Mixtures of Isomeric Dicarboxylic Acids

2013 ◽  
Vol 125 (21) ◽  
pp. 5614-5618 ◽  
Author(s):  
Krunoslav Užarević ◽  
Ivan Halasz ◽  
Ivica Đilović ◽  
Nikola Bregović ◽  
Mirta Rubčić ◽  
...  
Keyword(s):  
Solid State ◽  
Molecular Recognition ◽  
Dicarboxylic Acids

scholarly journals Solid state and sub-cooled liquid vapour pressures of substituted dicarboxylic acids using Knudsen Effusion Mass Spectrometry (KEMS) and Differential Scanning Calorimetry

2010 ◽  
Vol 10 (10) ◽  
pp. 4879-4892 ◽  
Author(s):  
A. M. Booth ◽  
M. H. Barley ◽  
D. O. Topping ◽  
G. McFiggans ◽  
A. Garforth ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Differential Scanning Calorimetry ◽  
Solid State ◽  
Dicarboxylic Acids ◽  
Estimation Methods ◽  
Scanning Calorimetry ◽  
Knudsen Effusion ◽  
Oh Groups ◽  
Knudsen Effusion Mass Spectrometry ◽  
The Impact

Abstract. Solid state vapour pressures of a selection of atmospherically important substituted dicarboxylic acids have been measured using Knudsen Effusion Mass Spectrometry (KEMS) over a range of 20 K (298–318 K). Enthalpies of fusion and melting points obtained using Differential Scanning Calorimetry (DSC) were used to obtain sub-cooled liquid vapour pressures. They have been compared to estimation methods used on the E-AIM website. These methods are shown to poorly represent – OH groups in combination with COOH groups. Partitioning calculations have been performed to illustrate the impact of the different estimation methods on organic aerosol mass compared to the use of experimental data.

scholarly journals Solid state and sub-cooled liquid vapour pressures of cyclic aliphatic dicarboxylic acids

2010 ◽  
Vol 10 (10) ◽  
pp. 23017-23043 ◽  
Author(s):  
A. M. Booth ◽  
W. J. Montague ◽  
M. H. Barley ◽  
D. O. Topping ◽  
G. McFiggans ◽  
...  
Keyword(s):  
Solid State ◽  
Dicarboxylic Acids ◽  
Estimation Methods ◽  
Melting Points ◽  
Straight Chain ◽  
Scanning Calorimetry ◽  
Knudsen Effusion ◽  
Knudsen Effusion Mass Spectrometry ◽  
First Time ◽  
Selection Of

Abstract. Knudsen Effusion Mass Spectrometry (KEMS) has been used to measure for the first time the solid state vapour pressures of a series of aliphatic cyclic dicarboxylic acids with increasing ring size. Additionally the atmospherically important compounds; cis-pinonic acid and levoglucosan were also measured. Differential Scanning Calorimetry (DSC) was used to measure melting points, enthalpies and entropies of fusion, which were used to determine sub-cooled liquid vapour pressures for the compounds. The sub-cooled liquid vapour pressure of straight chain, branched and cyclic dicarboxylic acids was compared to a selection of estimation methods.

scholarly journals Solid state and sub-cooled liquid vapour pressures of substituted dicarboxylic acids using Knudsen Effusion Mass Spectrometry (KEMS) and Differential Scanning Calorimetry

2010 ◽  
Vol 10 (2) ◽  
pp. 5717-5749
Author(s):  
A. M. Booth ◽  
M. H. Barley ◽  
D. O. Topping ◽  
G. McFiggans ◽  
A. Garforth
Keyword(s):  
Mass Spectrometry ◽  
Differential Scanning Calorimetry ◽  
Solid State ◽  
Dicarboxylic Acids ◽  
Estimation Methods ◽  
Scanning Calorimetry ◽  
Knudsen Effusion ◽  
Oh Groups ◽  
Knudsen Effusion Mass Spectrometry ◽  
The Impact

Abstract. Solid state vapour pressures of a selection of substituted dicarboxylic acids have been measured using Knudsen Effusion Mass Spectrometry (KEMS). Enthalpies of fusion and melting points obtained using Differential Scanning Calorimetry (DSC) were used to obtain sub-cooled liquid vapour pressures. They have been compared to estimation methods used on the E-AIM website. These methods are shown to poorly represent -OH groups in combination with COOH groups. Partitioning calculations have been performed to illustrate the impact of the different estimation methods on organic aerosol mass compared to the use of experimental data.

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