scholarly journals Blue fluorescence from N,O-coordinated BF2 complexes having aromatic chromophores in solution and the solid state

2019 ◽  
Vol 18 (12) ◽  
pp. 2884-2892 ◽  
Author(s):  
Minoru Yamaji ◽  
Kazuhiro Tomonari ◽  
Keisuke Ikuma ◽  
Kenta Goto ◽  
Fumito Tani ◽  
...  
Keyword(s):  
Solid State ◽  
Crystal Structures ◽  
Photophysical Properties ◽  
Blue Fluorescence

N,O-Coordinated BF2 complexes (Ar@HCs) having aromatic (Ar) and heterocycle (HC) moieties were prepared, and their photophysical properties were investigated in solution and the solid state along with their crystal structures.

scholarly journals Extended π-Systems in Diimine Ligands in [Cu(P^P)(N^N)][PF6] Complexes: From 2,2′-Bipyridine to 2-(Pyridin-2-yl)Quinoline

Crystals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 255 ◽  
Author(s):  
Sarah Keller ◽  
Murat Alkan-Zambada ◽  
Alessandro Prescimone ◽  
Edwin C. Constable ◽  
Catherine E. Housecroft
Keyword(s):  
Solid State ◽  
Crystal Structures ◽  
Photophysical Properties ◽  
Coordination Environment ◽  
Face To Face ◽  
Diimine Ligands ◽  
Structural Database ◽  
The Impact ◽  
Packing Effects

We describe the synthesis and characterization of [Cu(POP)(1)][PF6], [Cu(POP)(2)][PF6], [Cu(xantphos)(1)][PF6], and [Cu(xantphos)(2)][PF6] in which ligands 1 and 2 are 2-(pyridin-2-yl)quinoline and 2-(6-methylpyridin-2-yl)quinoline, respectively. With 2,2'-bipyridine (bpy) as a benchmark, we assess the impact of the extended π-system on structural and solid-state photophysical properties. The single crystal structures of [Cu(POP)(2)][PF6], [Cu(xantphos)(1)][PF6], and [Cu(xantphos)(2)][PF6] were determined and confirmed a distorted tetrahedral copper(I) coordination environment in each [Cu(P^P)(N^N)]+ cation. The xanthene unit in [Cu(xantphos)(1)][PF6] and [Cu(xantphos)(2)][PF6] hosts the quinoline unit of 1, and the 6-methylpyridine group of 2. 1H NMR spectroscopic data indicate that these different ligand orientations are also observed in acetone solution. In their crystal structures, the [Cu(POP)(2)]+, [Cu(xantphos)(1)]+, and [Cu(xantphos)(2)]+ cations exhibit different edge-to-face and face-to-face π-interactions, but in all cases, the copper(I) centre is effectively protected by a ligand sheath. In [Cu(POP)(2)][PF6], pairs of cations engage in an efficient face-to-face π-stacking embrace, and we suggest that this may contribute to this compound having the highest photoluminescence quantum yield (PLQY = 21%) of the series. With reference to data from the Cambridge Structural Database, we compare packing effects and PLQY data for the complexes incorporating 2-(pyridin-2-yl)quinoline and 2-(6-methylpyridin-2-yl)quinoline, with those of the benchmark bpy-containing compounds. We also assess the effect that Cu⋯O distances in the {Cu(POP)} and {Cu(xantphos)} domains of [Cu(P^P)(N^N)][X] compounds have on solid-state PLQY values.

scholarly journals Functionalised Terpyridines and Their Metal Complexes—Solid-State Interactions

Chemistry ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 199-227
Author(s):  
Young Hoon Lee ◽  
Jee Young Kim ◽  
Sotaro Kusumoto ◽  
Hitomi Ohmagari ◽  
Miki Hasegawa ◽  
...  
Keyword(s):  
Solid State ◽  
Metal Complexes ◽  
Crystal Structures ◽  
Weak Interactions ◽  
Dispersion Interactions ◽  
Derivatives Of

Analysis of the weak interactions within the crystal structures of 33 complexes of various 4′-aromatic derivatives of 2,2′:6′,2″-terpyridine (tpy) shows that interactions that exceed dispersion are dominated, as expected, by cation⋯anion contacts but are associated with both ligand–ligand and ligand–solvent contacts, sometimes multicentred, in generally complicated arrays, probably largely determined by dispersion interactions between stacked aromatic units. With V(V) as the coordinating cation, there is evidence that the polarisation of the ligand results in an interaction exceeding dispersion at a carbon bound to nitrogen with oxygen or fluorine, an interaction unseen in the structures of M(II) (M = Fe, Co, Ni, Cu, Zn, Ru and Cd) complexes, except when 1,2,3-trimethoxyphenyl substituents are present in the 4′-tpy.

Syntheses, Crystal Structures and Photophysical Properties of Dinuclear Copper(I) Complexes Bearing Diphenylphosphino‐Substituted Benzimidazole Ligands

2021 ◽  
Vol 6 (9) ◽  
pp. 2156-2163
Author(s):  
Mengmeng Cao ◽  
Yi Zhao ◽  
Mengsi Gu ◽  
Chunmei Liu ◽  
Qianqian Zhu ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Photophysical Properties ◽  
Dinuclear Copper

scholarly journals Fluorinated azobenzenes as supramolecular halogen-bonding building blocks

2019 ◽  
Vol 15 ◽  
pp. 2013-2019 ◽  
Author(s):  
Esther Nieland ◽  
Oliver Weingart ◽  
Bernd M Schmidt
Keyword(s):  
Solid State ◽  
Dft Calculations ◽  
Visible Light ◽  
Half Life ◽  
Photophysical Properties ◽  
Bathochromic Shift ◽  
Halogen Bonding ◽  
Building Blocks ◽  
Partial Overlap

ortho-Fluoroazobenzenes are a remarkable example of bistable photoswitches, addressable by visible light. Symmetrical, highly fluorinated azobenzenes bearing an iodine substituent in para-position were shown to be suitable supramolecular building blocks both in solution and in the solid state in combination with neutral halogen bonding acceptors, such as lutidines. Therefore, we investigate the photochemistry of a series of azobenzene photoswitches. Upon introduction of iodoethynyl groups, the halogen bonding donor properties are significantly strengthened in solution. However, the bathochromic shift of the π→π* band leads to a partial overlap with the n→π* band, making it slightly more difficult to address. The introduction of iodine substituents is furthermore accompanied with a diminishing thermal half-life. A series of three azobenzenes with different halogen bonding donor properties are discussed in relation to their changing photophysical properties, rationalized by DFT calculations.

Bis(1-phenyl-1-propyne) complexes of tungsten(II): crystal structures of [WI2(CO)(NCR)(η2-MeC2Ph)2] (R = Me, Et, or Ph)

2001 ◽  
Vol 79 (3) ◽  
pp. 263-271
Author(s):  
Paul K Baker ◽  
Michael GB Drew ◽  
Deborah S Evans
Keyword(s):  
Carbon Monoxide ◽  
Solid State ◽  
Crystal Structures ◽  
Octahedral Geometry ◽  
X Ray ◽  
X Ray Crystallography ◽  
Alkyne Complexes ◽  
First Time

Reaction of [WI2(CO)3(NCMe)2] with two equivalents of 1-phenyl-1-propyne (MeC2Ph) in CH2Cl2, and in the absence of light, gave the bis(1-phenyl-1-propyne) complex [WI2(CO)(NCMe)(η2-MeC2Ph)2] (1) in 77% yield. Treatment of equimolar quantities of 1 and NCR (R = Et, i-Pr, t-Bu, Ph) in CH2Cl2 afforded the nitrile-exchanged products, [WI2(CO)(NCR)(η2-MeC2Ph)2] (2-5) (R = Et (2), i-Pr (3), t-Bu (4), Ph (5)). Complexes 1, 2, and 5 were structurally characterized by X-ray crystallography. All three structures have the same pseudo-octahedral geometry, with the equatorial sites being occupied by cis and parallel alkyne groups, which are trans to the cis-iodo groups. The trans carbon monoxide and acetonitrile ligands occupy the axial sites. In structures 1 and 2, the methyl and phenyl substituents of the 1-phenyl-1-propyne ligands are cis to each other, whereas for the bulkier NCPh complex (5), the methyl and phenyl groups are trans to one another. This is the first time that this arrangement has been observed in the solid state in bis(alkyne) complexes of this type.Key words: bis(1-phenyl-1-propyne), carbonyl, nitrile, diiodo, tungsten(II), crystal structures.

Novel Pyridinium Inner Salt Dye and its Complexes: Synthesis, Crystal Structures and Photophysical Properties

2015 ◽  
Vol 25 (2) ◽  
pp. 473-479 ◽  
Author(s):  
Yong-Hong Zhou ◽  
Na-Li Wang ◽  
Ti-Fang Miao ◽  
Juan-Gang Wang ◽  
Zhe-Yu Wang
Keyword(s):  
Crystal Structures ◽  
Photophysical Properties

scholarly journals NOTIZEN. Weitere Verbindungen vom Typ A3NO3: K3NO3 und Rb3NO3 / Further Compounds Typ A3NO3: K3NO3 and Rb3NO3

1980 ◽  
Vol 35 (2) ◽  
pp. 237-238 ◽  
Author(s):  
Martin Jansen
Keyword(s):  
Solid State ◽  
Crystal Structures ◽  
Solid State Reaction ◽  
X Ray

Abstract K3NO3 and RbsNO3 were prepared by solid state reaction of equimolar mixtures of K2O/KNO2 and Rb20/RbN02, respectively. According to X-ray powder photographs their crystal structures are derived from the perovs-kite structure. K3NO3 is isostructural with Na3NO3 (a = 521.7 pm, Z = 1), Rb3NO3 represents a tetragonally distorted variant with a = 770.5, c = 550.8 pm and Z = 2.

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