scholarly journals Nine-ring angular fused biscarbazoloanthracene displaying a solid state based excimer emission suitable for OLED application

2016 ◽  
Vol 4 (24) ◽  
pp. 5795-5805 ◽  
Author(s):  
Gleb V. Baryshnikov ◽  
Pawel Gawrys ◽  
Khrystyna Ivaniuk ◽  
Bernhard Witulski ◽  
Richard J. Whitby ◽  
...  
Keyword(s):  
Solid State ◽  
Single Layer ◽  
Single Component ◽  
Excimer Emission ◽  
First Time

For the first time a fused polyaromatic compound is used for a single-layer single component WOLED.

Room-temperature white and color-tunable afterglow by manipulating multi-mode triplet emissions

2021 ◽  
Vol 9 (9) ◽  
pp. 3257-3263
Author(s):  
Jianwei Liu ◽  
Zhimin Ma ◽  
Zewei Li ◽  
Yan Liu ◽  
Xiaohua Fu ◽  
...  
Keyword(s):  
Room Temperature ◽  
Single Component ◽  
Color Tunable ◽  
First Time ◽  
Multi Mode

Two isomers pDCzPyCN and oDCzPyCN are designed and synthesized. Amazingly, oDCzPyCN manifest white afterglow at room temperature. This is the first time that single-component white afterglow has finally been realized.

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.

Single-component small-molecule white light organic phosphors

2017 ◽  
Vol 53 (66) ◽  
pp. 9269-9272 ◽  
Author(s):  
Ning-Ning Zhang ◽  
Cai Sun ◽  
Xiao-Ming Jiang ◽  
Xiu-Shuang Xing ◽  
Yong Yan ◽  
...  
Keyword(s):  
Solid State ◽  
Small Molecule ◽  
White Light ◽  
Light Emission ◽  
White Light Emission ◽  
Single Component ◽  
Supramolecular Aggregate ◽  
Organic Phosphors

A family of two small and easily synthesizable 1,2,3-triazole molecules with intrinsic white-light-emission in the solid state has been reported. The white light is assigned to the supramolecular aggregate emission (SAE) that is unusual for single-component white light phosphors.

Gold(I) Complexes Bearing P∩N-Ligands: An Unprecedented Twelve-membered Ring Structure Stabilized by Aurophilic Interactions

2009 ◽  
Vol 64 (11-12) ◽  
pp. 1513-1524 ◽  
Author(s):  
Uwe Monkowius ◽  
Manfred Zabel ◽  
Michel Fleck ◽  
Hartmut Yersin
Keyword(s):  
Solid State ◽  
Ring Structure ◽  
Phosphine Ligands ◽  
X Ray Crystallography ◽  
Aggregation Pattern ◽  
Elemental Analyses ◽  
High Yields ◽  
First Time ◽  
Solid State Structures ◽  
Aurophilic Interactions

The P∩N-ligands Ph2Pqn, 1, Ph2 Piqn, 2, Ph2 Ppym, 3, and the As∩N-ligands Ph2Asqn, 4, Ph2Asiqn, 5, (Ph = phenyl, qn = 8-quinoline, iqn = 1-isoquinoline, pym = 2-pyrimidine) have been synthesized, the ligands 2 and 5 for the first time. Their ligand properties were probed by the synthesis of gold(I) complexes. Reaction with (tht)AuCl (tht = tetrahydrothiophene) yielded the chlorogold complexes Ph2RP-Au-Cl (R = qn, 6; iqn, 7; pym, 8) and Ph2RAs-Au-Cl (R = qn, 9; iqn, 10) in high yields. Further treatment of 7 and 8 with one equivalent of AgBF4 provided the complexes [(Ph2Piqn)Au]BF4, 11, [(Ph2Ppym)Au]BF4, 12, and [(Ph2Piqn)Au(tht)]BF4, 14. For comparison, the previously reported complex [(Ph2Ppy)Au]BF4 (py = pyridine), 13, was re-investigated. The compounds were characterized by elemental analyses, mass spectrometry and NMR spectroscopy. In addition, the solid-state structures of 2, 3, 6, 7, 9 - 14 have been determined by X-ray crystallography. The chloro-gold compounds crystallize in the common rod-like structure known from R3EAuCl (R = aryl, E = P, As) complexes without further aggregation via aurophilic interactions. In all cases the phosphine acts as a monodentate ligand. In the solid state compounds 11 - 13 feature an unprecedented cyclic trinuclear aggregation pattern, in which the Au(I) atoms are linearly coordinated by the bridging phosphine ligands forming a cyclic (P-Au-N)3 arrangement. The resulting twelvemembered ring is further stabilized by Au · · · Au interactions. Due to the presence of these Au · · · Au contacts, 11 - 13 are emissive in the solid state but not in solution

Perforation mechanics of UHMWPE soft ballistic sub-laminate and soft ballistic armor pack: A finite element study

2021 ◽  
pp. 089270572110420
Author(s):  
Bazle Z (Gama) Haque ◽  
John W Gillespie
Keyword(s):  
Finite Element ◽  
Single Layer ◽  
Areal Density ◽  
Element Model ◽  
Transverse Impact ◽  
Free Standing ◽  
Uhmwpe Fibers ◽  
Ballistic Limit Velocity ◽  
Definition Of ◽  
First Time

Soft-ballistic sub-laminate (SBSL) made from ultra-high molecular weight polyethylene (UHMWPE) fibers in [0/90] stacking sequence are the building block of a multi-layer soft-ballistic armor pack (SBAP, aka Soft Armor). A systematic study of the perforation dynamics of a single layer SBSL and several multi-layer SBAPs (2, 3, 4, 8, 16, 24, 32 layers) is presented for the first time in the literature. A previously validated finite element model of transverse impact on a single layer is used to study the perforation mechanics of multi-layer SBAPs with friction between individual layers. Following the classical definition of ballistic limit velocity, a minimum perforation velocity has been determined for free-standing single layer SBSL and multi-layer SBAPs. For the multi-layer SBAPs, complete perforations have been identified as progressive perforation of individual layers through the thickness. The minimum perforation velocities of multi-layer SBAPS is linear with the areal density for the eight (8) layer target and thicker. Large deformation behavior and perforation mechanics of the SBAPs is discussed in detail.

Metal–organic cage-based nanoagent for enhanced photodynamic antitumor therapy

2021 ◽  
Author(s):  
Yu-Bin Dong ◽  
Wen-Yan Li ◽  
Chaowei Zhao ◽  
Yue-Feng Zhang ◽  
Qun Guan ◽  
...  
Keyword(s):  
Solid State ◽  
Indocyanine Green ◽  
Anion Exchange ◽  
Near Infrared ◽  
Antitumor Therapy ◽  
Metal Organic ◽  
First Time

Herein we report, for the first time, a Pd6L8(NO3)5.4(ICG)6.6 (ICG = indocyanine green) cage-based hexagonal nanoplate (3) via a combined nanoprecipitation and solid-state anion-exchange approach. 3 possesses near infrared (NIR)...

scholarly journals Revisiting the bis(dimethylamido) metallocene complexes of thorium and uranium: improved syntheses, structure, spectroscopy, and redox energetics of (C5Me5)2An(NMe2)2 (An = Th, U)

2017 ◽  
Vol 46 (34) ◽  
pp. 11208-11213 ◽  
Author(s):  
K. A. Erickson ◽  
B. D. Kagan ◽  
B. L. Scott ◽  
D. E. Morris ◽  
J. L. Kiplinger
Keyword(s):  
Solid State ◽  
Uv Visible ◽  
First Time ◽  
Solid State Structures ◽  
Metallocene Complexes

In addition to improved syntheses, the solid-state structures, voltammetric data and UV-visible–NIR spectra of (C5Me5)2An(NMe2)2 (An = Th, U) complexes are presented for the first time.

Niobium-bearing arsenides and germanides from elemental mixtures not involving niobium: a new twist to an old problem in solid-state synthesis

2018 ◽  
Vol 74 (5) ◽  
pp. 623-627 ◽  
Author(s):  
Sviatoslav Baranets ◽  
Hua He ◽  
Svilen Bobev
Keyword(s):  
High Temperature ◽  
Solid State ◽  
Diffraction Data ◽  
Alkaline Earth ◽  
Alkaline Earth Metals ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Temperature Reactions ◽  
First Time ◽  
Synthetic Work

Three isostructural transition-metal arsenides and germanides, namely niobium nickel arsenide, Nb0.92(1)NiAs, niobium cobalt arsenide, NbCoAs, and niobium nickel germanide, NbNiGe, were obtained as inadvertent side products of high-temperature reactions in sealed niobium containers. In addition to reporting for the very first time the structures of the title compounds, refined from single-crystal X-ray diffraction data, this article also serves as a reminder that niobium containers may not be suitable for the synthesis of ternary arsenides and germanides by traditional high-temperature reactions. Synthetic work involving alkali or alkaline-earth metals, transition or early post-transition metals, and elements from groups 14 or 15 under such conditions may yield Nb-containing products, which at times could be the major products of such reactions.

Influence of mixing energy on the solid-state behavior and clay fraction threshold of PA12/C30B® nanocomposites

2019 ◽  
Vol 39 (6) ◽  
pp. 565-572
Author(s):  
Nourredine Aït Hocine ◽  
Pascal Médéric ◽  
Hanaya Hassan
Keyword(s):  
Solid State ◽  
Mechanical Energy ◽  
Three Dimensional ◽  
Clay Fraction ◽  
Critical Value ◽  
Processing Conditions ◽  
State Behavior ◽  
Mixing Energy ◽  
End Use ◽  
First Time

Abstract This study focuses on the influence of mixing energy on the solid-state behavior and clay fraction threshold of nanocomposites. Thus, three polyamide12/clay (PA12/C30B®) nanocomposites exhibiting different nanostructures were prepared from three sets of processing conditions. Then, thermal and dynamical viscoelastic properties of these nanocomposites were analyzed, in relationship with the material nanostructure and processing conditions. For the first time, the solid-state properties of the nanocomposites revealed the existence of a critical specific mixing mechanical energy. Below this critical value, an increase of mechanical energy refines the structure, improving some end-use properties of the nanocomposite. Above this value, a high mixing energy supply is necessary in order to significantly modify the structure. They also highlighted that the clay fraction threshold, which is commonly attributed to the formation of a three-dimensional percolated network, decreases with increasing specific mixing energy, less significantly when this energy is superior to its critical value.

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