Meeting the Challenging Magnetic and Electronic Structure of Thiophene-Based Heterophenoquinones

Two thiophene-based heterophenoquinones, representing a family of molecules that exhibit biradicaloid character, have been studied by a combination of electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR), Raman, infrared (IR), and synchrotron or single-crystal X-ray diffraction measurements. This combined approach provided a detailed picture of the previously unknown electronic structure of the molecules in terms of two nearby states: a closed-shell diamagnetic state and a nearby biradical state, which is thermally populated.

[1]  E. Parisini,et al.  Outside rules inside: the role of electron-active substituents in thiophene-based heterophenoquinones. , 2015, Physical chemistry chemical physics : PCCP.

[2]  Run‐Wei Li,et al.  para-Quinodimethane-bridged perylene dimers and pericondensed quaterrylenes: the effect of the fusion mode on the ground states and physical properties. , 2014, Chemistry.

[3]  Jishan Wu,et al.  Zethrenes, extended p-quinodimethanes, and periacenes with a singlet biradical ground state. , 2014, Accounts of chemical research.

[4]  Claude Ruget,et al.  Developments in optics and performance at BL13-XALOC, the macromolecular crystallography beamline at the Alba Synchrotron , 2014, Journal of synchrotron radiation.

[5]  P. E. Keivanidis,et al.  Triple bulk heterojunctions as means for recovering the microstructure of photoactive layers in organic solar cell devices , 2014 .

[6]  G. Zerbi,et al.  Theoretical investigation and computational evaluation of overtone and combination features in resonance Raman spectra of polyenes and carotenoids , 2014 .

[7]  E. Canesi,et al.  Tuning the quinoid versus biradicaloid character of thiophene-based heteroquaterphenoquinones by means of functional groups. , 2012, Journal of the American Chemical Society.

[8]  T. Kubo,et al.  Aromaticity and π-bond covalency: prominent intermolecular covalent bonding interaction of a Kekulé hydrocarbon with very significant singlet biradical character. , 2012, Chemical communications.

[9]  Debra J. Mascaro,et al.  Spin-enhanced organic bulk heterojunction photovoltaic solar cells , 2012, Nature Communications.

[10]  D. Hashizume,et al.  Thickness Dependence of the Ambipolar Charge Transport Properties in Organic Field-Effect Transistors based on a Quinoidal Oligothiophene Derivative , 2011 .

[11]  E. Canesi,et al.  Biradicaloid character of thiophene-based heterophenoquinones: the role of electron-phonon coupling. , 2010, Chemphyschem : a European journal of chemical physics and physical chemistry.

[12]  G. Lanzani,et al.  A planar organic near infrared light detector based on bulk heterojunction of a heteroquaterphenoquinone and poly[2-methoxy-5-(2′-ethyl-hexyloxy)-1, 4-phenylene vinylene] , 2008 .

[13]  T. Kubo,et al.  Biradicaloid character of phenalenyl-based aromatic compounds with a small HOMO-LUMO gap , 2005 .

[14]  Y. Aso,et al.  Extensive quinoidal oligothiophenes with dicyanomethylene groups at terminal positions as highly amphoteric redox molecules. , 2005, Journal of the American Chemical Society.

[15]  W. M. Westler,et al.  Paramagnetic NMR spectroscopy and density functional calculations in the analysis of the geometric and electronic structures of iron-sulfur proteins. , 2005, Inorganic chemistry.

[16]  Hyoyoung Lee,et al.  Singlet-triplet gap in triplet ground-state biradicals is modulated by substituent effects. , 2002, Journal of the American Chemical Society.

[17]  J. Geus,et al.  Evidence for a new type of vanadyl pairs in (VO)2P2O7: an ESR and magnetisation study , 1998 .

[18]  K. Yanagi,et al.  Synthesis of Novel Heteroquaterphenoquinones and Their Electrochemical, Structural, and Spectroscopic Characterization. , 1996, The Journal of organic chemistry.

[19]  O. Kahn,et al.  Ferromagnetic spin alignment in molecular systems: an orbital approach , 1993 .

[20]  D. Dougherty Spin Control in Organic Molecules , 1991 .

[21]  Kazuko Takahashi,et al.  p-Diphenoquinone analogs extended by dihydrothiophenediylidene insertion. A novel amphoteric multistage redox system , 1989 .

[22]  J. Koutecký,et al.  OCCUPATION NUMBERS OF NATURAL ORBITALS AS A CRITERION FOR BIRADICAL CHARACTER. DIFFERENT KINDS OF BIRADICALS , 1980 .