Tuning solid state luminescent properties in a hydrogen bonding-directed supramolecular assembly of bis-cyclometalated iridium(iii) ethylenediamine complexes

2012 ◽  
Vol 41 (16) ◽  
pp. 4919 ◽  
Author(s):  
Anna Maria Talarico ◽  
Elisabeta Ildyko Szerb ◽  
Teresa F. Mastropietro ◽  
Iolinda Aiello ◽  
Alessandra Crispini ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Solid State ◽  
Supramolecular Assembly ◽  
Luminescent Properties

scholarly journals {N 1-[2-(Butylselanyl)benzyl]-N 2,N 2-dimethylethane-1,2-diamine}dichloridomercury(II)

2018 ◽  
Vol 74 (8) ◽  
pp. 1151-1154
Author(s):  
Pushpendra Singh ◽  
Harkesh B. Singh ◽  
Ray J. Butcher
Keyword(s):  
Hydrogen Bonding ◽  
Solid State ◽  
Self Assembly ◽  
Title Compound ◽  
Supramolecular Assembly ◽  
Molecular Geometry ◽  
The Self ◽  
Intermolecular Hydrogen Bonding ◽  
Hydrogen Bonding Interactions ◽  
Donor Acceptor

In the title compound, [HgCl2(C16H28N2Se)], the primary geometry around the Se and Hg atoms is distorted trigonal–pyramidal and distorted square-pyramidal, respectively. The distortion of the molecular geometry in the complex is caused by the steric demands of the ligands attached to the Se atom. The Hg atom is coordinated through two chloride anions, an N atom and an Se atom, making up an unusual HgNSeCl2 coordination sphere with an additional long Hg...N interaction. Intermolecular C—H...Cl interactions are the only identified intermolecular hydrogen-bonding interactions that seem to be responsible for the self assembly. These relatively weak C—H...Cl hydrogen bonds possess the required linearity and donor–acceptor distances. They act as molecular associative forces that result in a supramolecular assembly along the b-axis direction in the solid state of the title compound.

scholarly journals Synthesis and Structural Characterization of a Silver(I) Pyrazolato Coordination Polymer

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1015
Author(s):  
Kiyoshi Fujisawa ◽  
Takuya Nemoto ◽  
Yui Morishima ◽  
Daniel B. Leznoff
Keyword(s):  
Solid State ◽  
Coordination Polymer ◽  
Emission Spectra ◽  
Supramolecular Assembly ◽  
Luminescent Properties ◽  
Spectroscopic Properties ◽  
Coinage Metal ◽  
Argentophilic Interactions ◽  
Linear Coordination

Coinage metal(I)···metal(I) interactions are widely of interest in fields such as supramolecular assembly and unique luminescent properties, etc. Only two types of polynuclear silver(I) pyrazolato complexes have been reported, however, and no detailed spectroscopic characterizations have been reported. An unexpected synthetic method yielded a polynuclear silver(I) complex [Ag(μ-L1Clpz)]n (L1Clpz− = 4-chloride-3,5-diisopropyl-1-pyrazolate anion) by the reaction of {[Ag(μ-L1Clpz)]3}2 with (nBu4N)[Ag(CN)2]. The obtained structure was compared with the known hexanuclear silver(I) complex {[Ag(μ-L1Clpz)]3}2. The Ag···Ag distances in [Ag(μ-L1Clpz)]n are slightly shorter than twice Bondi’s van der Waals radius, indicating some Ag···Ag argentophilic interactions. Two Ag–N distances in [Ag(μ-L1Clpz)]n were found: 2.0760(13) and 2.0716(13) Å, and their N–Ag–N bond angles of 180.00(7)° and 179.83(5)° indicate that each silver(I) ion is coordinated by two pyrazolyl nitrogen atoms with an almost linear coordination. Every five pyrazoles point in the same direction to form a 1-D zig-zag structure. Some spectroscopic properties of [Ag(μ-L1Clpz)]n in the solid-state are different from those of {[Ag(μ-L1Clpz)]3}2 (especially in the absorption and emission spectra), presumably attributable to this zig-zag structure having longer but differently arranged intramolecular Ag···Ag interactions of 3.39171(17) Å. This result clearly demonstrates the different physicochemical properties in the solid-state between 1-D coordination polymer and metalacyclic trinuclear (hexanuclear) or tetranuclear silver(I) pyrazolate complexes.

Rietveld refinement of the cocrystal 2,4-dihydroxybenzoic acid–N′-(propan-2-ylidene)nicotinohydrazide (1/1)

2012 ◽  
Vol 68 (9) ◽  
pp. o335-o337 ◽  
Author(s):  
Saul H. Lapidus ◽  
Andreas Lemmerer ◽  
Joel Bernstein ◽  
Peter W. Stephens
Keyword(s):  
Hydrogen Bond ◽  
Hydrogen Bonding ◽  
Powder Diffraction ◽  
Supramolecular Assembly ◽  
Covalent Bond ◽  
Analytical Tool ◽  
Powder Diffraction Data ◽  
Dihydroxybenzoic Acid ◽  
Bond Forming ◽  
Hydrogen Bond Interactions

A further example of using a covalent-bond-forming reaction to alter supramolecular assembly by modification of hydrogen-bonding possibilities is presented. This concept was introduced by Lemmerer, Bernstein & Kahlenberg [CrystEngComm(2011),13, 55–59]. The title structure, C9H11N3O·C7H6O4, which consists of a reacted niazid molecule,viz.N′-(propan-2-ylidene)nicotinohydrazide, and 2,4-dihydroxybenzoic acid, was solved from powder diffraction data using simulated annealing. The results further demonstrate the relevance and utility of powder diffraction as an analytical tool in the study of cocrystals and their hydrogen-bond interactions.

Luminescent Properties of LiTaO3:Tm3+, Yb3+ Phosphors Prepared by Ball Milling Method

2013 ◽  
Vol 423-426 ◽  
pp. 426-429
Author(s):  
Xin Ze Wang ◽  
Zhong Xin Liu ◽  
Hong Jian Gao ◽  
Yani Jing ◽  
Chang Lin Li ◽  
...  
Keyword(s):  
Solid State ◽  
Ball Milling ◽  
Solid State Reaction ◽  
Blue Emission ◽  
Photoluminescence Property ◽  
Luminescent Properties ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Conventional Solid State Reaction ◽  
Energy Ball

LiTaO3: Tm3+, Yb3+powders were synthesized by a high-energy ball-milling (HEB) method compared with the conventional solid-state reaction (SSR) method. Under the excitation of 980 nm laser, the strong blue emission (477 nm) band is observed and attributed to1G4-3H6of Tm3+. Because of it causing high local temperature and narrow particles size, increasing the contact area between the particles and improved crystallinity of the host, synthesis by high-energy ball milling show higher photoluminescence (PL) intensity compared to the solid state reaction method. In the process of mechanical milling, Tm3+, Yb3+co-doped LiTaO3phosphors with high photoluminescence property could be achieved at a relatively low reaction temperature.

Sign in / Sign up

Export Citation Format

Share Document