Lithium heterocuprates: the influence of the amido group on organoamidocuprate structures

2014 ◽  
Vol 43 (38) ◽  
pp. 14359-14367 ◽  
Author(s):  
Roberta Bomparola ◽  
Robert P. Davies ◽  
Stefan Hornaeur ◽  
Andrew J. P. White

The structural isomers of a number of lithium heteroamidocuprates LiCuR(NR′2) have been studied in the solid state and in solution, with the steric and electronic properties of the amido group (NR′2) shown to significantly influence the solid-state structures and the position of the solution equilibrium.

2020 ◽  
Author(s):  
Jordann A.L. Wells ◽  
Muhammad Anwar Shameem ◽  
Arvind Kumar Gupta ◽  
Andreas Orthaber

The heterofulvenoid cyclopentadithiophene-phosphaalkene is a versatilie building block for opto-electronic tuning with donor and acceptor moieties. Both the annulated thienyl rings and the phosphaalkene bond can be functionalised using a variety of chemical transfomations, e.g. forming C-C, C-E (E = Si, Br) bonds or oxidation and metal coordination, respectively. Solid-state structures, optical and electronic properties are probed theoretically and experimentally, illustrating the opto-electronic tailoring opportunities at this motif.


Crystals ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 36 ◽  
Author(s):  
Hawazen Hassanain ◽  
E. Stephen Davies ◽  
William Lewis ◽  
Deborah L. Kays ◽  
Neil R. Champness

Functionalization of 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) chromophores at the 2,6-positions with iodo substituents and morpholino-substituted α-methyl groups affords molecules with strong absorbance in the visible spectrum. The effect of such substitution on the solid-state arrangements, absorption, fluorescence and electronic properties of these dye molecules is reported. The spectroscopic and spectroelectrochemical measurements display intense absorptions in the UV-visible spectrum with bathochromic shifts, in comparison to unfunctionalized BODIPY, and a positive shift in redox potentials due to functionalisation of the BODIPY core. Halogen bonds are observed in the solid-state structures of both halogenated BODIPY species, which in one case leads to the formation of an unusual halogen bonded framework.


2020 ◽  
Author(s):  
Jordann A.L. Wells ◽  
Muhammad Anwar Shameem ◽  
Arvind Kumar Gupta ◽  
Andreas Orthaber

The heterofulvenoid cyclopentadithiophene-phosphaalkene is a versatilie building block for opto-electronic tuning with donor and acceptor moieties. Both the annulated thienyl rings and the phosphaalkene bond can be functionalised using a variety of chemical transfomations, e.g. forming C-C, C-E (E = Si, Br) bonds or oxidation and metal coordination, respectively. Solid-state structures, optical and electronic properties are probed theoretically and experimentally, illustrating the opto-electronic tailoring opportunities at this motif.


2020 ◽  
Vol 59 (23) ◽  
pp. 17171-17183
Author(s):  
Sandra Schraff ◽  
Jens Trampert ◽  
Andreas Orthaber ◽  
Frank Pammer

Polymer ◽  
2004 ◽  
Vol 45 (12) ◽  
pp. 4009-4015 ◽  
Author(s):  
Bin Zhang ◽  
Shanju Zhang ◽  
Lidia Okrasa ◽  
Tadeusz Pakula ◽  
Tim Stephan ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document