On the Use of Solomon Echoes in 27Al NMR Studies of Complex Aluminium Hydrides

On the Use of Solomon Echoes in 27Al NMR Studies of Complex Aluminium Hydrides**

For two complex aluminium hydrides, the quadrupole coupling parameters of the 27Al nuclei are determined from static NMR spectra and compared with those obtained from MAS NMR spectra and from DFT-GIPAW calculations based on structural data from diffraction methods.


Abstract

The quadrupole coupling constant C Q and the asymmetry parameter η have been determined for two complex aluminium hydrides from 27Al NMR spectra recorded for stationary samples by using the Solomon echo sequence. The thus obtained data for KAlH4 (C Q=(1.30±0.02) MHz, η=(0.64±0.02)) and NaAlH4 (C Q=(3.11±0.02) MHz, η<0.01) agree very well with data previously determined from MAS NMR spectra. The accuracy with which these parameters can be determined from static spectra turned out to be at least as good as via the MAS approach. The experimentally determined parameters (δ iso, C Q and η) are compared with those obtained from DFT-GIPAW (density functional theory – gauge-including projected augmented wave) calculations. Except for the quadrupole coupling constant for KAlH4, which is overestimated in the GIPAW calculations by about 30 %, the agreement is excellent. Advantages of the application of the Solomon echo sequence for the measurement of less stable materials or for in situ studies are discussed.

H2Open – Guest Editorial

H2Open – Guest Editorial

H2Open is a special collection of research articles and reviews focused on the multifaceted chemistry of water from different scientific vantage points. Guest editors Mihail Barboiu, Barbara Kirchner, Eva Perlt and Alessandro Scarso give an overview of the collection.


Abstract

This special collection presents original research articles and reviews that are connected to the multifaceted and rich chemistry of water. These works serve as an illustration of how, despite its apparent simplicity and ubiquity, water continues to be at the center of scientific exploration from a wide range of perspectives and employing the toolbox of modern-day chemistry.

Synthesis and Properties of Twisted and Helical Azulene Oligomers and Azulene‐Based Polycyclic Hydrocarbons

Synthesis and Properties of Twisted and Helical Azulene Oligomers and Azulene-Based Polycyclic Hydrocarbons

Twisted or helical shape 1,2-position-connected terazulene and quaterazulene were synthesized. Variable temperature NMR measurements and theoretical calculations of the quaterazulene suggest that the syn-type structure with terminal azulene overlap is more stable. Planar or bent shape fused terazulenes were also synthesized. Nucleus-independent chemical shift (NICS) calculations carried out for the central seven-membered ring of the bent shape fused terazulene showed a positive value, suggesting anti-aromatic properties.


Abstract

The construction of 1,2-position-connected azulene oligomers was achieved. In the crystal packing structure of the terazulene, two molecules of (R a)- and (S a)-configurations formed a pair. Variable temperature NMR measurements and theoretical calculations of the quaterazulene suggest that the helical and syn-type structure with terminal azulene overlap is more stable. Two kinds of fused terazulenes (1,2′′-closed and 1,8′′-closed) were also synthesized by intramolecular Pd-catalyzed C−H/C−Br arylation of the terazulene moieties. X-ray structure analysis of 1,2′′-closed terazulene revealed a planar structure, while an analysis of 1,8′′-closed terazulene performed on a C60 co-crystal revealed a curved structure forming a 1 : 1 complex covering the co-crystal. Nucleus-independent chemical shift (NICS) calculations carried out for the central seven-membered ring of 1,8′′-closed terazulene showed a positive value, suggesting anti-aromatic properties.

Imidazolyl‐Substituted Benzo‐ and Naphthodithiophenes as Precursors for the Synthesis of Transient Open‐Shell Quinoids

Imidazolyl-Substituted Benzo- and Naphthodithiophenes as Precursors for the Synthesis of Transient Open-Shell Quinoids

A series of sulfur-containing heteroacenes were synthesized and utilized as precursors to imidazolylidene-substituted quinoids. The transiently formed quinoids exhibit small singlet-triplet gaps and exist as open-shell molecules, as evidenced by EPR spectroscopy and quantum chemical calculations.


Abstract

The synthesis of three novel imidazolyl-substituted sulfur-containing heteroacenes is reported. These heteroacenes consisting of annelated benzo- and naphthothiophenes serve as precursors for the generation of open-shell quinoid heteroacenes by oxidation with alkaline ferric cyanide. Spectroscopic and computational experiments support the formation of reactive open-shell quinoids, which, however, quickly produce paramagnetic polymeric material.