40102-86-1Relevant articles and documents
Microporous thioxanthone polymers as heterogeneous photoinitiators for visible light induced free radical and cationic polymerizations
Dadashi-Silab, Sajjad,Bildirir, Hakan,Dawson, Robert,Thomas, Arne,Yagci, Yusuf
, p. 4607 - 4614 (2014)
Conjugated microporous polymeric networks possessing thioxanthone groups were reported to initiate free radical and cationic polymerizations of vinyl monomers and cyclic ethers, respectively, under visible light irradiation. These new classes of Type II macrophotoinitiators with high porosity having large BET surface area of 500-750 m2 g-1 were prepared through different cross-coupling processes. Polymerizations are successfully achieved in conjugation with several co-initiators benefiting from hydrogen abstraction or electron transfer reactions stimulated by either visible light or natural sunlight irradiation. Photopolymerizations conducted by using knitted photoinitiators show better conversion and rate of polymerization than those obtained via Sonogashira-Hagihara coupling. The heterogeneous nature of the photoinitiators makes them easily separable from the media and more importantly reusable for further polymerizations while retaining the photocatalytic activity.
Catalyst-Controlled Stereoselective Barton–Kellogg Olefination
Schmidt, Tanno A.,Sparr, Christof
, p. 23911 - 23916 (2021/10/08)
Overcrowded alkenes are expeditiously prepared by the versatile Barton–Kellogg olefination and have remarkable applications as functional molecules owing to their unique stereochemical features. The induced stereodynamics thereby enable the controlled motion of molecular switches and motors, while the high configurational stability prevents undesired isomeric scrambling. Bistricyclic aromatic enes are prototypical overcrowded alkenes with outstanding stereochemical properties, but their stereocontrolled preparation was thus far only feasible in stereospecific reactions and with chiral auxiliaries. Herein we report that direct catalyst control is achieved by a stereoselective Barton–Kellogg olefination with enantio- and diastereocontrol for various bistricyclic aromatic enes. Using Rh2(S-PTAD)4 as catalyst, several diazo compounds were selectively coupled with a thioketone to give one of the four anti-folded overcrowded alkene stereoisomers upon reduction. Complete stereodivergence was reached by catalyst control in combination with distinct thiirane reductions to provide all four stereoisomers with e.r. values of up to 99:1. We envision that this strategy will enable the synthesis of topologically unique overcrowded alkenes for functional materials, catalysis, energy- and electron transfer, and bioactive compounds.
Non-Planar and Flexible Hole-Transporting Materials from Bis-Xanthene and Bis-Thioxanthene Units for Perovskite Solar Cells
Urieta-Mora, Javier,García-Benito, Inés,Zimmermann, Iwan,Aragó, Juan,García-Fernández, Pedro D.,Grancini, Giulia,Molina-Ontoria, Agustín,Ortí, Enrique,Martín, Nazario,Nazeeruddin, Mohammad Khaja
, (2019/04/13)
Two new hole-transporting materials (HTMs), BX-OMeTAD and BTX-OMeTAD, based on xanthene and thioxanthene units, respectively, and bearing p-methoxydiphenylamine peripheral groups, are presented for their use in perovskite solar cells (PSCs). The novelty of the newly designed molecules relies on the use of a single carbon-carbon bond ‘C?C’ as a linker between the two functionalized heterocycles, which increases the flexibility of the molecule compared with the more rigid structure of the widely used HTM spiro-OMeTAD. The new HTMs display a limited absorbance in the visible region, due to the lack of conjugation between the two molecular halves, and the chemical design used has a remarkably impact on the thermal properties when compared to spiro-OMeTAD. BX-OMeTAD and BTX-OMeTAD have been tested in ([(FAPbI3)0.87(MAPbBr3)0.13]0.92[CsPbI3]0.08)-based PSC devices exhibiting power conversion efficiencies of 14.19 and 16.55 %, respectively. The efficiencies reached, although lower than those measured for spiro-OMeTAD (19.63 %), are good enough to consider the chemical strategy used as an interesting via to design HTMs for PSCs.
Organic compound having tetrahedron-like configuration
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Paragraph 0156; 0162; 0164; 0165, (2018/07/07)
The present invention relates to an organic compound having a tetrahedron-like configuration, wherein the organic compound has a structure represented by the following general formula (I) defined in the specification, A1-A4 are respectively and independently an unsaturated five-membered ring or an unsaturated six-membered ring, B is a direct bond , -C, -O-, -N-, -S-, or -C=C-, m is 0 or 1, Ris hydrogen, fluorine, substituted or unsubstituted C1-C12 alkyl, or substituted or unsubstituted C6-C12 aryl, and n is an integer of 0-2. The organic compound of the present invention has excellentphotoelectric property.
