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Tatiana V Timofeeva

Publications and source records attributed to Tatiana V Timofeeva.

10 recordsLinked to original sources

Synthesis, ionisation potentials and electron affinities of hexaazatrinaphthylene derivatives.

Several hexaazatrinaphthylene derivatives and a tris(thieno)hexaazatriphenylene derivative have been synthesised by reaction of the appropriate diamines with hexaketocyclohexane. The crystal structure of 2,3,8,9,14,15-hexachloro-5,6,11,12,17,18-hexaazatrinaphthylene has been determined by X-ray diffraction; this reveals a molecular structure in good agreement with that predicted by density functional theory (DFT) calculations and pi-stacking with an average spacing between adjacent molecular planes of 3.18 A. Solid-state ionisation potentials have been measured by using UV photoelectron spectroscopy and fall in the range of 5.99 to 7.76 eV, whereas solid-state electron affinities, measured using inverse photoelectron spectroscopy, vary in the range -2.65 to -4.59 eV. The most easily reduced example is a tris(thieno)hexaazatriphenylene substituted with bis(trifluoromethyl)phenyl groups; DFT calculations suggest that the highly exothermic electron affinity is due both to the replacement of the outermost phenylene rings of hexaazatrinaphthylene with thieno groups and to the presence of electron-withdrawing bis(trifluoromethyl)phenyl groups. The rather exothermic electron affinities, the potential for adopting pi-stacked structures and the low intramolecular reorganisation energies obtained by DFT calculations suggest that some of these molecules may be useful electron-transport materials.

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Hexaferrocenylbenzene.

Hexaferrocenylbenzene has been synthesized by six-fold Negishi type ferrocenylation of hexabromo- or hexaiodobenzene.

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Isolation and crystal structures of two singlet bis(triarylamine) dications with nonquinoidal geometries.

We report the first structural data for bis(diarylamine) "bipolarons": we have isolated and crystallographically characterized salts of the dications obtained by two-electron oxidation of E-4,4'-bis[di(p-anisyl)amino]stilbene and E,E-2,5-bis{4-[di(p-anisyl)amino]styryl}-3,4-di(n-butoxy)thiophene, [1](2+) and [2](2+) respectively. ESR, NMR, and magnetometry suggest both species have singlet ground states. X-ray structures, together with (1)H NMR coupling constants for [2](2+), indicate geometries in which the bond lengths are shifted toward a quinoidal pattern relative to that in the neutral species, but not to a fully quinoidal extent. In particular, the bond-length alternations across the vinylene bridging groups approach zero. DFT calculations with closed-shell singlet configurations reproduce the observed structures well. Our results indicate that singlet species for which one might expect quinoidal geometries (with differences of ca. 0.1 A between formally single and double bonds) on the basis of a limiting valence-bond representation of the structure can, in fact, show structures with significantly different patterns of bond lengths.

Aniline Compounds↗

Role of donor-acceptor strengths and separation on the two-photon absorption response of cytotoxic dyes: a TD-DFT study.

Time-dependent density functional theory (TD-DFT) is applied to model one-photon (OPA) and two-photon (TPA) absorption spectra in a series of conjugated cytotoxic dyes. Good agreement with available experimental data is found for calculated excitation energies and cross sections. Calculations show that both OPA and TPA spectra in the molecules studied are typically dominated by two strong peaks corresponding to different electronic states. We find that donor-acceptor strengths and conjugated bridge length have a strong impact on the cross-section magnitudes of low- and high-frequency TPA maxima, respectively. These trends are analyzed in terms of the natural transition orbitals of the corresponding electronic states. Observed structure-property relationships may have useful implications on design of organic conjugated chromophores with tunable two-photon absorption properties for photodynamic therapy applications.

Absorption↗

Difurazano[3,4-b:3',4'-f]-4,5-diaza-1,8-dioxacyclododecine and an acyclic analogue.

The novel title furazan-containing macrocycle (systematic name: 6,9,14,17-tetraoxa-2,3,5,7,16,18-hexaazatricyclo[13.3.0.0(4,8)]octadeca-4,7,15,18-tetraene), C8H10N6O4, (I), is the first macrocycle where the furazan rings are connected via a hydrazine group. In spite of the strain in the 12-membered macrocycle of (I), the geometry of the furazan fragment is the same in (I) and in its acyclic analogue 1,8-bis(5-aminofurazan-4-yloxy)-3,6-dioxaoctane, C10H16N6O6, (II). In both compounds, the participation of the furazan rings in intermolecular hydrogen bonding equalizes the N-O bonds within the furazan rings, in contrast with rings which do not participate in such interactions.

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3,5-bis[4-(diethylamino)benzylidene]-1-methyl-4-piperidone and 3,5-bis[4-(diethylamino)cinnamylidene]-1-methyl-4-piperidone: prospective biophotonic materials.

The structures of 3,5-bis[4-(diethylamino)benzylidene]-1-methyl-4-piperidone, C(28)H(37)N(3)O, (I), and 3,5-bis[4-(diethylamino)cinnamylidene]-1-methyl-4-piperidone, C(32)H(41)N(3)O, (II), have been characterized. Because of conjugation between donor and acceptor parts, the central heterocycles (including the carbonyl group) in (I) and (II) are flattened and exhibit a 'sofa' conformation, with a deviation of the N atom from the planar fragment. The dihedral angles between the planar part of the heterocycle and the two almost flat fragments that include a phenyl ring and bridging atoms are 23.2 (1) and 11.2 (1) degrees in (I), and 11.8 (1) and 8.7 (2) degrees in (II). One- and two-photon absorption of light and the fluorescence of (I) and (II) have also been characterized.

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N,N-dimethyl-N'-[(1E,2E)-3-(4-nitrophenyl)prop-2-enylidene]benzene-1,4-diamine and N,N-dimethyl-4-[(1E,3E)-4-(4-nitrophenyl)buta-1,3-dienyl]-1-naphthylamine.

Syntheses and X-ray structural investigations have been carried out for the two title compounds, viz. C(17)H(17)N(3)O(2), (I), and C(22)H(20)N(2)O(2), (II). The molecular skeleton of (I) is slightly non-planar; the dihedral angles between the conjugated linkage and the p-(dimethylamino)phenyl ring, and between the linkage and the p-nitrophenyl ring are 13.0 (2) and 13.8 (2) degrees, respectively. The dihedral angle between the slightly pyramidal dimethylamine substituent and the aromatic ring is 23.3 (1) degrees. The molecular skeleton of (II) is not planar; the dihedral angles between the conjugated linkage and the naphthalene ring, and between the linkage and the substituted phenyl ring are 36.1 (2) and 2.7 (3) degrees, respectively. The dimethylamine substituent in (II) has a pyramidal geometry; the dihedral angle between this substituent and the naphthalene ring is 71.7 (1) degrees. The dihedral angle between the nitro group and the plane of the substituted phenyl ring is 9.0 (3) degrees. There is a weak intermolecular C-H.O hydrogen bond in the crystal structure of (II), which links the molecules into centrosymmetric dimers. Molecular mechanics calculations of molecular conformations have shown that the crystal environment influences the conformation more in (I) than in (II).

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Four 3-cyanodifurazanyl ethers: potential propellants.

In earlier papers, we described the synthesis and structures of bis(3-nitrofurazan-4-yl) ether, C(4)N(6)O(7), (I), bis[3-(nitro-N,N,O-azoxy)furazan-4-yl] ether, C(4)N(10)O(9), (II), and bis[3-(5H-[1,2,3]triazolo[4,5-c]furazan-5-yl)furazan-4-yl] ether, C(8)N(14)O(5), (III). Here we compare the structures of (I)-(III) with those of four 3-cyanodifurazanyl ethers, namely bis(3-cyanofurazan-4-yl) ether, C(6)N(6)O(3), (IV), 3-cyanofurazanyl 3-nitrofurazanyl ether, C(5)N(6)O(5), (V), 3,4-bis(3-cyanofurazan-4-yloxy)furazan, C(8)N(8)O(5), (VI), and bis[3-(3-cyanofurazan-4-yloxy)furazan-4-yl]diazene, C(10)N(12)O(6), (VII). It was found that the geometric parameters of the difurazanyl ether fragments are similar in these structures and therefore not influenced by substituent effects; however, the conformation of this fragment is different, viz. structures (I), (III), (V) and (VI) have approximate C(2) symmetry, and structures (II), (IV) and (VII) have C(s) symmetry. Dense crystal packing (1.626-1.898 Mg m(-3)) is characteristic for all these hydrogen-free compounds. A linear correlation is also determined between crystal density and 'molecular density' (M/V), where M is the mass of a molecule and V is the molecular volume.

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(E)-(4-hydroxyphenyl)(4-nitrophenyl)diazene, (E)-(4-methoxyphenyl)(4-nitrophenyl)diazene and (E)-[4-(6-bromohexyloxy)phenyl](4-cyanophenyl)diazene.

Syntheses and X-ray structural investigations have been carried out for (E)-(4-hydroxyphenyl)(4-nitrophenyl)diazene, C(12)H(9)N(3)O(3), (Ia), (E)-(4-methoxyphenyl)(4-nitrophenyl)diazene, C(13)H(11)N(3)O(3), (IIIa), and (E)-[4-(6-bromohexyloxy)phenyl](4-cyanophenyl)diazene, C(19)H(20)BrN(3)O, (IIIc). In all of these compounds, the molecules are almost planar and the azobenzene core has a trans geometry. Compound (Ia) contains four and compound (IIIc) contains two independent molecules in the asymmetric unit, both in space group P1 (No. 2). In compound (Ia), the independent molecules are almost identical, whereas in crystal (IIIc), the two independent molecules differ significantly due to different conformations of the alkyl tails. In the crystals of (Ia) and (IIIa), the molecules are arranged in almost planar sheets. In the crystal of (IIIc), the molecules are packed with a marked separation of the azobenzene cores and alkyl tails, which is common for the solid crystalline precursors of mesogens.

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Three polar derivatives of N-ethylcarbazole: materials for optical applications.

Three N-ethylcarbazole derivatives have been synthesized and tested for non-linear optical (NLO) properties. The compounds are 2-(9-ethyl-9H-carbazol-3-ylmethylene)malononitrile, C(18)H(13)N(3), (IIIa), 2-cyano-3-(9-ethyl-9H-carbazol-3-yl)thioacrylamide, C(18)H(15)N(3)S, (IIIb), and 3-(9-ethyl-9H-carbazol-3-yl)-2-(4-phenyl-1,3-thiazol-2-yl)acrylonitrile, C(26)H(19)N(3)S, (V). It was found that the molecules of (IIIa) and (V) are nearly planar, while non-planarity is more pronounced for (IIIb). Molecules of (IIIa) and (V) exhibit herring-bone packing motifs. In (IIIb), the molecules form layers coplanar with (-201), within which they form centrosymmetric dimers via N-H...S hydrogen bonds.

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