Susceptibility of two-dimensional resonance Raman spectroscopies to cascades involving solute and solvent molecules

2019 ◽  
Vol 151 (10) ◽  
pp. 104203
Author(s):  
Thomas P. Cheshire ◽  
Andrew M. Moran
2015 ◽  
Vol 143 (12) ◽  
pp. 124202 ◽  
Author(s):  
Zhenkun Guo ◽  
Brian P. Molesky ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

2016 ◽  
Vol 145 (3) ◽  
pp. 034203 ◽  
Author(s):  
Brian P. Molesky ◽  
Zhenkun Guo ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

2017 ◽  
Vol 375 (6) ◽  
Author(s):  
Zhenkun Guo ◽  
Brian P. Molesky ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

2016 ◽  
Vol 145 (18) ◽  
pp. 180901 ◽  
Author(s):  
Brian P. Molesky ◽  
Zhenkun Guo ◽  
Thomas P. Cheshire ◽  
Andrew M. Moran

1993 ◽  
Vol 47 (9) ◽  
pp. 1343-1344 ◽  
Author(s):  
Ken Ebihara ◽  
Hiroaki Takahashi ◽  
Isao Noda

Nanosecond two-dimensional resonance Raman spectroscopy was used to investigate the photochemistry of the production and decay of the radical anion of benzil in various solvents. A newly developed correlation formalism was applied to a set of time-resolved resonance Raman spectra of the benzil radical anion to generate two-dimensional Raman spectra. Unlike the 2D correlation method previously developed for IR spectroscopy, which was based on signals induced by a sinusoidally varying external perturbation, the new correlation formalism is generally applicable to the studies of any transient spectroscopic signals having an arbitrary waveform. This makes it ideally suited for the analysis of time-resolved spectroscopic signals following photoexcitation. 2D Raman spectra effectively accentuate certain useful information which is sometimes obscured in the original time-resolved spectra. Spectral intensity changes and peak shifts arising from the photochemical reaction processes were clearly observed by the synchronous and asynchronous correlation.


2016 ◽  
Vol 72 (6) ◽  
pp. 480-484 ◽  
Author(s):  
Qiu-Ying Huang ◽  
Xiao-Yi Lin ◽  
Xiang-Ru Meng

The N-heterocyclic ligand 2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole (imb) has a rich variety of coordination modes and can lead to polymers with intriguing structures and interesting properties. In the coordination polymercatena-poly[[cadmium(II)-bis[μ-benzene-1,2-dicarboxylato-κ4O1,O1′:O2,O2′]-cadmium(II)-bis{μ-2-[(1H-imidazol-1-yl)methyl]-1H-benzimidazole}-κ2N2:N3;κ2N3:N2] dimethylformamide disolvate], {[Cd(C8H4O4)(C11H10N4)]·C3H7NO}n, (I), each CdIIion exhibits an irregular octahedral CdO4N2coordination geometry and is coordinated by four O atoms from two symmetry-related benzene-1,2-dicarboxylate (1,2-bdic2−) ligands and two N atoms from two symmetry-related imb ligands. Two CdIIions are connected by two benzene-1,2-dicarboxylate ligands to generate a binuclear [Cd2(1,2-bdic)2] unit. The binuclear units are further connected into a one-dimensional chain by pairs of bridging imb ligands. These one-dimensional chains are further connected through N—H...O hydrogen bonds and π–π interactions, leading to a two-dimensional layered structure. The dimethylformamide solvent molecules are organized in dimeric pairsviaweak interactions. In addition, the title polymer exhibits good fluorescence properties in the solid state at room temperature.


2014 ◽  
Vol 70 (2) ◽  
pp. m35-m35
Author(s):  
Jing-Wei Dai ◽  
Zhao-Yang Li ◽  
Osamu Sato

In the title complex, [Fe(NCS)2(C18H18N4)], the FeIIcation is chelated by a tris(2-pyridylmethyl)amine ligand and coordinated by two thiocyanate anions in a distorted N6octahedral geometry. In the crystal, weak C—H...S hydrogen bonds and π–π stacking interactions between parallel pyridine rings of adjacent molecules [centroid–centroid distance = 3.653 (3) Å] link the molecules into a two-dimensional supramolecular architecture. The structure contains voids of 124 (9) Å3, which are free of solvent molecules.


2020 ◽  
Vol 75 (4) ◽  
pp. 341-345
Author(s):  
Xiao-Li Liu ◽  
Jing-Long Liu ◽  
Hong-Mei Yang ◽  
Ai-Quan Jia ◽  
Qian-Feng Zhang

AbstractCo-crystallization of C-propyl-pyrogallol[4]arene (PgC3) with 4,4′-bipyridine (bpy) in ethanol afforded a multi-component complex (PgC3) · 3(bpy) ·(EtOH) (1) that consists of a one-dimensional brick-wall framework, which was formed by four pyrogallol[4]arene molecules and two juxtaposed bpy molecules, entrapping two other bpy molecules as guests within each cavity. Heating a mixture of PgC3 and trans-1,2-bis-(4-pyridyl)ethylene (bpe) in an ethanol-water mixed solvent allowed the isolation of a multi-component complex (PgC3) ·(bpe) · 2(EtOH) ·(H2O) (2), which has a two-dimensional wave-like polymer structure with the bpe molecules embedded in the wave trough between two PgC3 molecules. Single-crystal X-ray crystallography was utilized to investigate the hydrogen bonding networks of the multi-component complexes 1 and 2.


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