RESUMEN
We explored the optoelectronic and vibrational properties of a new class of halogen-terminated carbon atomic wires in the form of polyynes using UV-vis, infrared absorption, Raman spectroscopy, X-ray single-crystal diffraction, and DFT calculations. These polyynes terminate on one side with a cyanophenyl group and on the other side, with a halogen atom X (X = Cl, Br, I). We focus on the effect of different halogen terminations and increasing lengths (i.e., 4, 6, and 8 sp-carbon atoms) on the π-electron conjugation and the electronic structure of these systems. The variation in the sp-carbon chain length is more effective in tuning these features than changing the halogen end group, which instead leads to a variety of solid-state architectures. Shifts between the vibrational frequencies of samples in crystalline powders and in solution reflect intermolecular interactions. In particular, the presence of head-to-tail dimers in the crystals is responsible for the modulation of the charge density associated with the π-electron system, and this phenomenon is particularly important when strong I··· N halogen bonds occur.
RESUMEN
This study shows the first example of cycloaddition-retro-electrocyclization (CA-RE) click reaction involving nitrogen end-capped push-pull oligoynes. The reported CA-RE reaction with TCNE (tetracyanoethylene) is fully regioselective and leads exclusively to the unprecedented TCBD (tetracyanobuta-1,3-diene-2,3-diyl) end-capped carbon rods. The molecular structure of the products was unambiguously confirmed using X-ray single crystal diffraction and their optical and electronic properties were investigated experimentally and rationalized using DFT (density functional theory) calculations.
RESUMEN
A supramolecular trilayer nanographene complex consisting of a newly synthesized D3h-symmetric C54-nanographene trisimide (NTI 1) and two hexabenzocoronenes (HBC) has been obtained by self-assembly. This 1:2 complex is structurally well-defined according to UV/vis and single crystal X-ray studies and exhibits high thermodynamic stability even in polar halogenated solvents. Complexation of NTI 1 by two HBC molecules protects the NTI 1 π-surface efficiently from oxygen quenching, thereby leading to a sequestration-induced fluorescence enhancement under ambient conditions.
Asunto(s)
Fluorescencia , Solventes/química , TermodinámicaRESUMEN
Synthesis of complex di(selenophen-3-yl)diselenides and 3-methylene-3H-1,2-diselenoles directly from 1-bromobutadiynes is described. The transformation is performed under conditions used before for the synthesis of simple selenophenes from butadiynes. The reaction is operationally straightforward, and complex products were obtained in high yields. Structures of the final products were unambiguously confirmed by the means of 77Se NMR and single-crystal X-ray diffraction.
RESUMEN
The first planar π-extended azulene that retains aromaticity of odd-membered rings was synthesized by [3+3] peri-annulation of two naphthalene imides at both long-edge sides of azulene. Using bromination and subsequent nucleophilic substitution by methoxide and morpholine, selective functionalization of the π-extended azulene was achieved. Whilst these new azulenes can be regarded as isomers of terrylene bisimide they exhibit entirely different properties, which include very narrow optical and electrochemical gaps. DFT, TD-DFT, as well as nucleus-independent chemical shift calculations were applied to explain the structural and functional properties of these new πâ scaffolds. Furthermore, X-ray crystallography confirmed the planarity of the reported π-scaffolds and aromaticity of their azulene moiety.
RESUMEN
The reaction of bis(triphenylphosphine)iridium(i) carbonyl chloride (Vaska's complex) with a series of 1-iodopolyynes (1-CnI and 2-CnI) gave σ-polyynyl iridium(iii) complexes with general formula R(C[triple bond, length as m-dash]C)nIr(PPh3)2(Cl)(I)(CO). The use of acetonitrile as a solvent appeared crucial and allowed selectively obtaining only one from a few possible isomers. The X-ray single crystal diffraction experiment for 2-C4[Ir]I allowed the determination of the exact structure of this complex. Further spectroscopic measurements, especially 31P NMR, confirmed the formation of the same type of isomers with trans coordinated phosphines in each case. All complexes were fully characterized with the use of NMR (1H, 13C and 31P), IR, UV/Vis, cyclic voltammetry and (ESI)HRMS techniques. Moreover, DFT calculations were performed for all the resulting species. The complexes with a linear carbon chain from butadiyne to decapentayne are the longest iridium end-capped polyynes known to date since only compounds with a (C[triple bond, length as m-dash]C)2 structural motif have been reported so far. Moreover, we confirmed that the synthetic approach, first used for palladium(ii) end-capped polyynes, may be also applied for the synthesis of other structurally new organometallic polyynes.
RESUMEN
The reactions of a series of 1-halopolyynes with secondary amines led to novel amine end-capped polyynes exhibiting surprisingly high stability toward moisture. The new compounds were characterized by NMR spectroscopy, ESI-MS spectrometry, and X-ray single-crystal diffractometry. The use of amine end-capped polyynes as precursors to substituted push-pull thiophenes was next presented. The results show the first-to the best of our knowledge-transformation of ynamine to thiophene and the first regioselective transformation of a longer polyynes to butadiyne-substituted thiophene. Photophysical studies of the resulting compounds show that some of the substituted thiophenes have high quantum yield photoluminescence upon UV light irradiation.
RESUMEN
In this contribution, the synthesis of long chain hexatriynyl- and octatetraynyl-substituted pyrroles in one step from 1-halopolyyne precursors is reported. The products were obtained via a mechanochemical approach by simple grinding of 1-haloalkynes with N-substituted pyrroles and potassium carbonate which played a role of heterogeneous catalyst and this solvent- and transition metal-free approach is unprecedent in the synthesis of new, organic, long chain polyynes. Additionally, an extensive X-ray single crystal study of pyrrole end-capped polyynes is presented. Such compounds are possible substrates for different oligoheterocycles and have a significant application potential such as for instance molecular wires.
RESUMEN
The synthesis of a unique series of long, asymmetric 1-iodopolyynes (1-Cn I and 2-Cn I) with the sp-hybridized carbon chain up to a decapentayne is reported. These compounds were then used as substrates in reactions with Pd(PPh3 )4 leading to another series of palladium end-capped polyynes, which were unstable in solution. Organometallic octatetraynes 1-C8 [Pd]I, 2-C8 [Pd]I, and decapentayne 1-C10 [Pd]I are palladium end-capped polyyne compounds with the longest carbon chains reported so far. All the complexes as well as their organic precursors were fully characterized by NMR, HRMS(ESI), IR, TGA-DTA, and UV/Vis techniques, and the X-ray crystal structures of two silyl-protected precursors and one palladium complex are presented. The synthetic approach for palladium species is envisioned as a general route for the synthesis of labile organometallic polyynes.
RESUMEN
A highly efficient one-pot procedure for the preparation of 1-chloroalkynes and 1-chlorobutadiynes from terminal and trialkylsilyl-protected precursors is reported. This convenient reaction, proceeding under mild conditions, utilizes N-chlorosuccinimide as the chlorinating agent and tolerates a range of functional groups.