ChemInform Abstract: INTERCONVERSION OF CIS-TRANS ISOMERS IN MX(CO)2(UNSYMMETRIC, BIDENTATE PHOSPHINE)2

1978 ◽  
Vol 9 (25) ◽  
Author(s):  
L. D. BROWN ◽  
S. DATTA ◽  
J. K. KOUBA ◽  
L. K. SMITH ◽  
S. S. WREFORD
Keyword(s):  
Trans Isomers ◽  
Bidentate Phosphine

Interconversion of cis-trans isomers in MX(CO)2(unsymmetric, bidentate phosphine)2

1978 ◽  
Vol 17 (3) ◽  
pp. 729-734 ◽  
Author(s):  
L. D. Brown ◽  
S. Datta ◽  
J. K. Kouba ◽  
L. K. Smith ◽  
S. S. Wreford
Keyword(s):  
Trans Isomers ◽  
Bidentate Phosphine

Ligand isomerism in Pt(II) complexes – structural aspects

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Milan Melník ◽  
Peter Mikuš
Keyword(s):  
Mixed Ligand ◽  
Bidentate Ligands ◽  
Trans Isomers ◽  
Mean Values ◽  
Bite Angle ◽  
Coordination Spheres ◽  
Structural Aspects

Abstract This review has focused on ligand isomers in Pt(II) complexes. There are a variety of inner coordination spheres about the platinum(II) atom (PtN4, PtN2Cl2, PtP2Cl2, PtPNC2, PtPNCl2, PtP2CBr, PtP2CS), build up by mono- and bidentate ligands. The bidentate ligands create a variety of metallocyclic rings. The L–Pt–L bite angle (mean values) open in the sequence: 73.1° (PNP) < 78.7° (NC2C) < 80.4° (NC2N) < 86.4° (PC2P) < 86.7° (PNNP) < 93.0° (CC3S). There are three types of isomers: ligand, mixed – (ligand + distortion), and mixed – (ligand + cis-trans), isomers, which are rarity.

scholarly journals cis-trans Isomers of Di-α-tocopherone

1964 ◽  
Vol 239 (2) ◽  
pp. 574-577
Author(s):  
A. Saari Csallany ◽  
H.H. Draper
Keyword(s):  
Trans Isomers

scholarly journals PSVII-18 Fatty acid composition of the longissimus muscle from Angus and Wagyu sired cattle at the 6th and 12th rib location

2020 ◽  
Vol 98 (Supplement_3) ◽  
pp. 211-212
Author(s):  
Jerad Jaborek ◽  
Francis L Fluharty ◽  
Alejandro E Relling
Keyword(s):  
Fatty Acid ◽  
Mixed Model ◽  
Random Effect ◽  
Repeated Measurements ◽  
Longissimus Muscle ◽  
Trans Isomers ◽  
Fa Composition ◽  
Effect Of Treatment ◽  
Similar Body ◽  
Location Interaction

Abstract The fatty acid (FA) composition of the longissimus muscle (LM) of Angus and Wagyu sired cattle raised to a similar body weight (612 kg) were compared at the 6th and 12th rib locations. Angus sired steers represented T1, cattle from a Wagyu sire selected for growth represented T2, and cattle from a Wagyu sire selected for marbling represented T3. Data were analyzed mixed model with repeated measurements on animal (LM location); the model include the fixed effect of treatment, LM location, and their interaction, and random effect of sex. The percentage of 16:0, 18:1cis9, 18:3, and monounsaturated FA (MUFA) exhibited a treatment*LM location interaction (P ≤ 0.7), where T2 cattle had a greater percentage of 16:0 and a lesser percentage of 18:1cis9, 18:3, and MUFA at the 12th rib vs. 6th rib location compared with T1 and T3 cattle. The percentage of total FA lipid, polyunsaturated FA(PUFA), and PUFA:SFA ratio in the LM were greater (P ≤ 0.02) for T3 cattle compared with T1 and T2 cattle. The percentage of 18:0 was greater (P ≤ 0.01) for T1 cattle compared with T2 and T3 cattle, while T1 cattle had a greater (P ≤ 0.01) percentage of saturated FA (SFA) compared to T3 cattle. The percentage of 18:1cis9, other 18:1cis isomers, 18:2, MUFA, and MUFA:SFA ratio were greater (P ≤ 0.02) for T3 cattle compared with T1 cattle, with T2 cattle being intermediate. The percentage of total FA lipid, 18:0, 18:1 trans isomers, and SFA were greater (P ≤ 0.01) at the 6th rib LM location, while 14:1, 18:cis9, other 18:1 cis isomers, MUFA, MUFA:SFA, and PUFA:SFA ratio were greater (P ≤ 0.02) at the 12th rib LM location

scholarly journals Identification of Anthocyanin Compounds in Butterfly Pea Flowers (Clitoria ternatea L.) by Ultra Performance Liquid Chromatography/Ultraviolet Coupled to Mass Spectrometry

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4539
Author(s):  
Nguyen Minh Thuy ◽  
Vo Minh ◽  
Tran Ben ◽  
My Tuyen Thi Nguyen ◽  
Ho Ha ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Liquid Chromatography ◽  
Ultra Performance Liquid Chromatography ◽  
Negative Ion ◽  
Trans Isomers ◽  
Clitoria Ternatea ◽  
Flower Extract ◽  
Cis And Trans Isomers ◽  
Butterfly Pea ◽  
Cis And Trans

Butterfly pea flower have great sensory attraction, but they have not yet been used widely in Vietnam. Extracts of butterfly pea flowers can be used conveniently as a natural blue colorant for food products. In this study, the identification of anthocyanin compounds in butterfly pea flowers was performed by UPLC coupled with a UV and Mass spectrometer instrument. Positive and negative ion electrospray MS/MS chromatograms and spectra of the anthocyanin compounds were determined. By analyzing the chromatograms and spectra for each ion, five anthocyanins were identified in the butterfly pea flower extract; these were delphinidin-3-(6”‐p-coumaroyl)-rutinoside, cyanidin 3-(6”-p-coumaroyl)-rutinoside, delphinidin-3-(p-coumaroyl) glucose in both cis- and trans- isomers, cyanidin-3-(p-coumaroyl-glucoside) and delphinidin-3-pyranoside. Additionally, based on their intensity, it was determined that cyanidin-3-(p-coumaroyl-glucoside) was the most abundant anthocyanin, followed by cyanidin 3-(6”-p-coumaroyl)-rutinoside, delphinidin-3-(p-coumaroyl-glucoside), delphinidin-3-(6”-p-coumaroyl)-rutinoside and delphinidin-3-pyranoside. In this study, cyanidin derivatives were discovered in butterfly pea flower extract, where these compounds had not been detected in previous studies.

Unveiling the coexistence of cis- and trans-isomers in the hydrolysis of ZrO2: A coupled DFT and high-resolution photoelectron spectroscopy study

2020 ◽  
Vol 153 (24) ◽  
pp. 244308
Author(s):  
Ali Abou Taka ◽  
Mark C. Babin ◽  
Xianghai Sheng ◽  
Jessalyn A. DeVine ◽  
Daniel M. Neumark ◽  
...  
Keyword(s):  
High Resolution ◽  
Photoelectron Spectroscopy ◽  
Spectroscopy Study ◽  
Trans Isomers ◽  
Cis And Trans Isomers ◽  
Cis And Trans ◽  
Hydrolysis Of

Darstellung, Schwingungsspektren und Normalkoordinatenanalyse von Chloro-Bromo-Rhodaten(III) / Preparation, Vibration Spectra and Normal Coordinate Analysis of Chloro-Bromo-Rhodates(III)

1989 ◽  
Vol 44 (10) ◽  
pp. 1221-1227 ◽  
Author(s):  
W. Preetz ◽  
W. Kuhr
Keyword(s):  
Exchange Chromatography ◽  
Trans Isomers ◽  
Normal Coordinate ◽  
Valence Force ◽  
Trans Influence ◽  
Diethylaminoethyl Cellulose ◽  
Point Groups ◽  
First Time ◽  
Ir And Raman ◽  
Good Agreement

The mixed chloro-bromo-rhodates(III) [RhClnBr6-n]3-, n = 1-5, have been separated for the first time by ion exchange chromatography on diethylaminoethyl-cellulose. Due to the stronger trans-effect of Br, as compared with Cl, on treatment of [RhBr6]3- with conc. HCl nearly pure cis/fac-isomers for n = 2, 3, 4 are formed. The reaction of [RhCl6]3- with conc. HBr yields mixtures of the cis/trans-isomers for n = 2, 4, which cannot be separated, but mer-[RhCl3Br3]3 is formed stereospecifically. The IR and Raman spectra of all isolated mixed ligand complexes are completely assigned according to point groups Oh, D3d, C4v, C3v and C2v, supported by normal coordinate analyses based on a general valence force field. The good agreement of calculated and observed frequencies confirms the assignments. Due to the stronger trans-influence of Br as compared to Cl, in all asymmetric Cl—Rh—Br axes the Rh—Br bonds are strengthened and the Rh—Cl bonds are weakened, indicated by valence force constants for Rh—Br approximately 14% higher, for Rh—Cl 10% lower, as compared with the values calculated for symmetric Br—Rh—Br and Cl—Rh—Cl axes, respectively.

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