Andere Kunden interessierten sich auch für
![Carbon Filled Conjugated Polymers]( "Carbon Filled Conjugated Polymers")
Carbon Filled Conjugated Polymers44,99 €![Conjugated Polymer Networks]( "Conjugated Polymer Networks")
Conjugated Polymer Networks44,99 €![-Cyclodextrin Conjugated Dendrimer]( "-Cyclodextrin Conjugated Dendrimer")
-Cyclodextrin Conjugated Dendrimer32,99 €![Polythiophene based conjugated polymer for optoelectronic application]( "Polythiophene based conjugated polymer for optoelectronic application")
Polythiophene based conjugated polymer for optoelectronic application44,99 €![Doping in Conjugated Polymers]( "Doping in Conjugated Polymers")
Doping in Conjugated Polymers155,99 €![Topological Approach to the Chemistry of Conjugated Molecules]( "Topological Approach to the Chemistry of Conjugated Molecules")
Topological Approach to the Chemistry of Conjugated Molecules40,99 €![New Conjugated Polymers Based on Benzodifuranone and Diketopyrrolopyrrole]( "New Conjugated Polymers Based on Benzodifuranone and Diketopyrrolopyrrole")
New Conjugated Polymers Based on Benzodifuranone and Diketopyrrolopyrrole69,50 €
A conjugated system occurs in an organic compound where atoms covalently bond with alternating single and multiple (e.g. double) bonds (e.g., C=C-C=C-C) and influence each other to produce a region called electron delocalization. In this region electrons do not belong to a single bond or atom, but rather a group. For example, phenol (C6H5OH, benzene with hydroxyl group) (diagramatically has lternating single and double bonds), which has a system of 6 electrons above and below the flat planar ring, as well as around the hydroxyl group. The conjugated system results in a general delocalization of the electrons across all of the adjacent parallel aligned p-orbitals of the atoms, which increases stability and thereby lowers the overall energy of the molecule.