The phrase "trans configuration" is grammatically correct and can be used in written English.
It is commonly used in chemistry and physics to describe the arrangement or orientation of molecules or objects. Example: The presence of a double bond in a molecule can result in a trans configuration, where the atoms on either side of the bond are on opposite sides.
In the trans configuration, the two adjacent carbons lie on opposite sides of the double-bonded carbons.
During hydrogenation some of the unsaturation is converted to the trans configuration, with like groups on opposite sides of the plane.
Simultaneously with the change of some of the unsaturation to the trans configuration there is a migration of double bonds along the chain.
The experimental spectrum revealed only one conformer with trans configuration and C1 symmetry.
The bulky ligand, 2-PhC6H4O-, promotesynhe syn conformation in the active site in favor of trans configuration in polybutadiene.
The main chain methylene carbons attached to the ring has a trans configuration for one of them and a cis arrangement for the other.
PXRD and solid-state NMR data confirmed lamellar structures, where the tilted hydrocarbon chains were crystallized in the fully extended all-trans configuration [20, 63].
For the precise discussion of the 7,8-s-trans configuration, we designed and synthesized the 7,8-cis-locked skeleton of vitamin D3 derivatives.
The second domain, which is thought to bind the xanthophyll molecule in the all-trans configuration, shows similarity to the eight-stranded β-barrel structure of the lipocalin protein family [38].
By absorption of a photon, 11-cis-retinal is isomerized to the all-trans configuration, resulting in the deprotonation of the retinylidene Schiff-base and the formation of the active, G protein-binding metarhodopsin II (Meta II) state.
Generation of correct disulfide bonds and peptidyl-prolyl cis-trans configuration are required processes for formation and stabilization of the native protein conformation.
