TY  - JOUR
A1  - Crumbach, Merian
A1  - Bachmann, Jonas
A1  - Fritze, Lars
A1  - Helbig, Andreas
A1  - Krummenacher, Ivo
A1  - Braunschweig, Holger
A1  - Helten, Holger
T1  - Dithiophene‐Fused Oxadiborepins and Azadiborepins: A New Class of Highly Fluorescent Heteroaromatics
JF  - Angewandte Chemie International Edition
N2  - Access to dithiophene‐fused oxadiborepins and the first azadiborepins attained via a modular synthesis route are presented. The new compounds emit intense blue light, some of which demonstrate fluorescence quantum yields close to unity. Cyclic voltammetry (CV) revealed electrochemically reversible one‐electron reduction processes. The weak aromatic character of the novel 1,2,7‐azadiborepin ring is demonstrated with in‐depth theoretical investigations using nucleus‐independent chemical shift (NICS) scans and anisotropy of the induced current density (ACID) calculations.
KW  - aromaticity
KW  - BN compounds
KW  - boron
KW  - isoelectronic analogues
KW  - polycycles
Y1  - 2021
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-238996
VL  - 60
IS  - 17
SP  - 9290
EP  - 9295
ER  - 
TY  - JOUR
A1  - Hagspiel, Stephan
A1  - Arrowsmith, Merle
A1  - Fantuzzi, Felipe
A1  - Vargas, Alfredo
A1  - Rempel, Anna
A1  - Hermann, Alexander
A1  - Brückner, Tobias
A1  - Braunschweig, Holger
T1  - Highly colored boron-doped thiazolothiazoles from the reductive dimerization of boron isothiocyanates
JF  - Angewandte Chemie International Edition
N2  - Reduction of (CAAC)BBr\(_2\)(NCS) (CAAC=cyclic alkyl(amino)carbene) in the presence of a Lewis base L yields tricoordinate (CAAC)LB(NCS) borylenes which undergo reversible E/Z-isomerization. The same reduction in the absence of L yields deep blue, bis(CAAC)-stabilized, boron-doped, aromatic thiazolothiazoles resulting from the dimerization of dicoordinate (CAAC)B(NCS) borylene intermediates.
KW  - inorganic chemistry
KW  - aromaticity
KW  - reduction
KW  - fused thiazaboroles
KW  - DFT
KW  - borylenes
Y1  - 2021
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-256432
VL  - 60
IS  - 12
ER  - 
TY  - JOUR
A1  - Roy, Dipak Kumar
A1  - Tröster, Tobias
A1  - Fantuzzi, Felipe
A1  - Dewhurst, Rian D.
A1  - Lenczyk, Carsten
A1  - Radacki, Krzysztof
A1  - Pranckevicius, Conor
A1  - Engels, Bernd
A1  - Braunschweig, Holger
T1  - Isolation and Reactivity of an Antiaromatic s‐Block Metal Compound
JF  - Angewandte Chemie International Edition
N2  - The concepts of aromaticity and antiaromaticity have a long history, and countless demonstrations of these phenomena have been made with molecules based on elements from the p, d, and f blocks of the periodic table. In contrast, the limited oxidation‐state flexibility of the s‐block metals has long stood in the way of their participation in sophisticated π‐bonding arrangements, and truly antiaromatic systems containing s‐block metals are altogether absent or remain poorly defined. Using spectroscopic, structural, and computational techniques, we present herein the synthesis and authentication of a heterocyclic compound containing the alkaline earth metal beryllium that exhibits significant antiaromaticity, and detail its chemical reduction and Lewis‐base‐coordination chemistry.
KW  - antiaromaticity
KW  - aromaticity
KW  - beryllium
KW  - heterocycles
KW  - s-block metals
Y1  - 2021
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-224447
VL  - 60
IS  - 7
SP  - 3812
EP  - 3819
ER  -