Applications of a New High Pressure Anvil Cell for IR Spectroscopy

Author(s):  
Edward G. Bartick
2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Michael Zoller ◽  
Hubert Huppertz

AbstractThe rare earth oxoborates REB5O8(OH)2 (RE = Ho, Er, Tm) were synthesized in a Walker-type multianvil apparatus at a pressure of 2.5 GPa and a temperature of 673 K. Single-crystal X-ray diffraction data provided the basis for the structure solution and refinement. The compounds crystallize in the monoclinic space group C2 (no. 5) and are composed of a layer-like structure containing dreier and sechser rings of corner sharing [BO4]5− tetrahedra. The rare earth metal cations are coordinated between two adjacent sechser rings. Further characterization was performed utilizing IR spectroscopy.


2015 ◽  
Vol 3 (22) ◽  
pp. 11976-11984 ◽  
Author(s):  
Haiyan Mao ◽  
Jun Xu ◽  
Yue Hu ◽  
Yining Huang ◽  
Yang Song

A first high-pressure study on MOF α-Mg3(HCOO)6 probed by in situ vibrational spectroscopy revealed strongly contrasting host-dependent structural transitions and stabilities.


1987 ◽  
Vol 42 (2) ◽  
pp. 187-196
Author(s):  
E. M. Borschel ◽  
M. Buback

Pivalic acid in dilute solution of n-heptane and of CCl4 is studied via IR spectroscopy in the region of the C = O and O - H stretching fundamentals up to pressures of 2 kbar and temperatures of 175 °C. Lambert-Beer's law is shown to be valid for the C = O modes of the acid monomer and of the hydrogen-bonded cyclic dimer, which enables the quantitative measurement of the dimerization equilibrium as a function of pressure and temperature. Increasing pressure favours the dimerization in n-heptane to a larger extent than in CCl4 solution. In both solvents this pressure effect increases with temperature. The hydrogen bond strength within the dimer species is slightly reduced toward high pressure. The data on the temperature dependence of the dimerization volume and on the pressure dependence of the dimerization enthalpy are compared with direct information on both species as derived from their O - H fundamental modes.


Langmuir ◽  
2011 ◽  
Vol 27 (8) ◽  
pp. 4728-4733 ◽  
Author(s):  
Zhimin Liu ◽  
André Rittermeier ◽  
Michael Becker ◽  
Kevin Kähler ◽  
Elke Löffler ◽  
...  

2004 ◽  
Vol 357 (15) ◽  
pp. 4537-4543 ◽  
Author(s):  
Maria Caporali ◽  
Piero Frediani ◽  
Antonella Salvini ◽  
Gabor Laurenczy

2017 ◽  
Vol 46 (9) ◽  
pp. 2821-2828 ◽  
Author(s):  
Stephen E. Repper ◽  
Anthony Haynes ◽  
Evert J. Ditzel ◽  
Glenn J. Sunley

Reversible formation of copper(i) carbonyl complexes from copper-containing ionic liquids is probed directly using in situ high pressure IR spectroscopy.


2015 ◽  
Vol 17 (33) ◽  
pp. 21143-21148 ◽  
Author(s):  
Hai-Chou Chang ◽  
Jyh-Chiang Jiang ◽  
Meng-Hsiu Kuo ◽  
Ding-Tsai Hsu ◽  
Sheng Hsien Lin

The formation of pressure-enhanced C–H⋯nano-TiO2 interactions around the C–H groups was observed.


2003 ◽  
Vol 27 (3) ◽  
pp. 283-295 ◽  
Author(s):  
Alberto Striolo ◽  
Alessandro Favaro ◽  
Nicola Elvassore ◽  
Alberto Bertucco ◽  
Vito Di Noto

2020 ◽  
Vol 75 (6-7) ◽  
pp. 605-613
Author(s):  
Daniela Vitzthum ◽  
Daniel S. Wimmer ◽  
Ingo Widmann ◽  
Hubert Huppertz

AbstractThe isotypic triel borates Al5B12O25(OH) and Ga4InB12O25(OH) were synthesized in a Walker-type multianvil apparatus under high-pressure/high-temperature conditions of 12.0 GPa/1400 °C and 12.3 GPa/1200 °C, respectively. The crystal structures of both compounds, determined by single-crystal X-ray diffraction, constitute new representatives of the structure type M5B12O25(OH) (M = Ga, In) crystallizing in the space group I41/acd. The presence of the hydroxyl groups was confirmed via single-crystal IR spectroscopy.


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