Broadband dielectric spectroscopic characterization of the hydrolytic degradation of carboxylic acid-terminated poly(d,l-lactide) materials

Polymer ◽  
2007 ◽  
Vol 48 (7) ◽  
pp. 2022-2029 ◽  
Author(s):  
Mohammad K. Hassan ◽  
Jeffrey S. Wiggins ◽  
Robson F. Storey ◽  
Kenneth A. Mauritz
Keyword(s):  
Carboxylic Acid ◽  
Hydrolytic Degradation ◽  
Spectroscopic Characterization

Synthesis and spectroscopic characterization of enantiopure protected trans-4-amino-1-oxyl-2,2,6,6-tetramethyl piperidine-3-carboxylic acid (trans β-TOAC)

2005 ◽  
Vol 46 (33) ◽  
pp. 5573-5576 ◽  
Author(s):  
Karen Wright ◽  
Augustin de Castries ◽  
Matthieu Sarciaux ◽  
Fernando Formaggio ◽  
Claudio Toniolo ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Spectroscopic Characterization

scholarly journals Benzyl and Phenyl Glucosinolates Are Metabolized by the Specific Plant Pathogen Alternaria Brassicicola but Not by the Generalist Fungal Pathogens Rhizoctonia Solani or Sclerotinia Sclerotiorum

2021 ◽  
Author(s):  
M. Soledade C. Pedras ◽  
Chintamani Thapa ◽  
Sajjad Hossain
Keyword(s):  
Carboxylic Acid ◽  
Rhizoctonia Solani ◽  
Sclerotinia Sclerotiorum ◽  
Plant Pathogen ◽  
Fungal Pathogens ◽  
Spectroscopic Characterization ◽  
Fungal Species ◽  
Alternaria Brassicicola ◽  
Metabolic Products

The metabolism of benzyl and phenyl glucosinolates by three phytopathogenic fungal species is investigated and established that <i>A. brassicicola </i>metabolized intact benzyl and phenyl glucosinolates and the corresponding desulfo derivatives. Syntheses and spectroscopic characterization of benzyl and phenyl desulfo-glucosinolates are reported. Phenylacetonitrile and benzylisothiocyanate are the first metabolic products of benzyl glucosinolate; benzyl isothiocyanate is further metabolized to 3-benzyl-2-thioxo-2,3-dihydrothiazolidine-4-carboxylic acid.

scholarly journals Crystallographic and spectroscopic characterization of (R)-O-acetylmandelic acid

2016 ◽  
Vol 72 (7) ◽  
pp. 901-903
Author(s):  
Cady Cirbes ◽  
Joseph M. Tanski
Keyword(s):  
Hydrogen Bonding ◽  
Carboxylic Acid ◽  
Mandelic Acid ◽  
Phenylacetic Acid ◽  
Spectroscopic Characterization ◽  
Acid Group ◽  
Intermolecular Hydrogen Bonding ◽  
Carboxylic Acid Group ◽  
Donor Acceptor

The title compound [systematic name: (R)-(−)-2-acetoxy-2-phenylacetic acid], C10H10O4, is a resolved chiral ester derivative of mandelic acid. The compound contains an acetate group and a carboxylic acid group, which engage in intermolecular hydrogen bonding, forming chains extending parallel to [001] with a short donor–acceptor hydrogen-bonding distance of 2.676 (2) Å.

scholarly journals Crystallographic and spectroscopic characterization of 4-nitro-2-(trifluoromethyl)benzoic acid and 4-nitro-3-(trifluoromethyl)benzoic acid

2019 ◽  
Vol 75 (4) ◽  
pp. 524-528
Author(s):  
George L. Diehl III ◽  
Lisa Je ◽  
Joseph M. Tanski
Keyword(s):  
Hydrogen Bonding ◽  
Carboxylic Acid ◽  
Benzoic Acid ◽  
Nitro Group ◽  
Spectroscopic Characterization ◽  
Acid Group ◽  
Carboxylic Acid Group ◽  
Donor Acceptor ◽  
Graph Set

The title compounds, both C8H4F3NO4, represent two isomers of nitro trifluoromethyl benzoic acid. The compounds each contain a nitro functionality para to the carboxylic acid group, with the trifluoromethyl substituent ortho to the acid group in the 2-isomer and ortho to the nitro group in the 3-isomer. The regiochemistry with respect to the trifluoromethyl group results in steric interactions that rotate the carboxylic acid group or the nitro group out of the aromatic plane in the 2- and 3-isomer, respectively. Each molecule engages in intermolecular hydrogen bonding, forming head-to-tail dimers with graph-set notation R 2 2(8) and donor–acceptor hydrogen-bonding distances of 2.7042 (14) Å in the 2-isomer and 2.6337 (16) in the 3-isomer. Recrystallization attempts did not yield untwinned crystals.

scholarly journals Benzyl and Phenyl Glucosinolates Are Metabolized by the Specific Plant Pathogen Alternaria Brassicicola but Not by the Generalist Fungal Pathogens Rhizoctonia Solani or Sclerotinia Sclerotiorum

2021 ◽  
Author(s):  
M. Soledade C. Pedras ◽  
Chintamani Thapa ◽  
Sajjad Hossain
Keyword(s):  
Carboxylic Acid ◽  
Rhizoctonia Solani ◽  
Sclerotinia Sclerotiorum ◽  
Plant Pathogen ◽  
Fungal Pathogens ◽  
Spectroscopic Characterization ◽  
Fungal Species ◽  
Alternaria Brassicicola ◽  
Metabolic Products

The metabolism of benzyl and phenyl glucosinolates by three phytopathogenic fungal species is investigated and established that <i>A. brassicicola </i>metabolized intact benzyl and phenyl glucosinolates and the corresponding desulfo derivatives. Syntheses and spectroscopic characterization of benzyl and phenyl desulfo-glucosinolates are reported. Phenylacetonitrile and benzylisothiocyanate are the first metabolic products of benzyl glucosinolate; benzyl isothiocyanate is further metabolized to 3-benzyl-2-thioxo-2,3-dihydrothiazolidine-4-carboxylic acid.

scholarly journals Crystallographic and spectroscopic characterization of racemic Mosher's Acid

2020 ◽  
Vol 76 (7) ◽  
pp. 1143-1145
Author(s):  
Carolyn Z. Savich ◽  
Joseph M. Tanski
Keyword(s):  
Carboxylic Acid ◽  
Spectroscopic Characterization ◽  
Acid Group ◽  
Compound C ◽  
Unit Form ◽  
Derivatizing Agent ◽  
Donor Acceptor ◽  
Group A ◽  
Mosher’S Acid

The title compound, C10H9F3O3, represents the structure of racemic Mosher's Acid (systematic name: 3,3,3-trifluoro-2-methoxy-2-phenylpropanoic acid), a carboxylic acid that when resolved can be employed as a chiral derivatizing agent. The compound contains a carboxylic acid group, a methoxy group and a trifluoromethyl substituent on an asymmetric benzylic carbon atom. The two independent molecules in the asymmetric unit form a non-centrosymmetric homochiral dimer via intermolecularly hydrogen-bonded head-to-tail dimers with graph-set notation R 2 2(8) and donor–acceptor hydrogen-bonding distances of 2.6616 (13) and 2.6801 (13) Å.

An irresolute linker: separation, and structural and spectroscopic characterization of the two linkage isomers of a Ru(ii)-(2-(2′-pyridyl)pyrimidine-4-carboxylic acid) complex

2014 ◽  
Vol 43 (32) ◽  
pp. 12160-12163 ◽  
Author(s):  
E. Iengo ◽  
N. Demitri ◽  
G. Balducci ◽  
E. Alessio
Keyword(s):  
Solid State ◽  
Carboxylic Acid ◽  
Spectroscopic Characterization ◽  
Acid Complex ◽  
Linkage Isomers ◽  
First Time

For the first time the two linkage isomers of a Ru(ii) complex with 2-(2′-pyridyl)pyrimidine-4-carboxylic acid (cppH) have been fully characterized individually, both in solution and in the solid state.

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