1-Methylphenanthro[3,4-b]thiophene: Determination of the tertiary structure in solution and in the crystalline state by NMR spectroscopy and X-ray diffraction

1985 ◽  
Vol 22 (2) ◽  
pp. 545-553 ◽  
Author(s):  
M. J. Musmar ◽  
Gary E. Martin ◽  
Robert T. Gampe ◽  
Vincent M. Lynch ◽  
Stanley H. Simonsen ◽  
...  
2017 ◽  
Vol 73 (3) ◽  
pp. 184-190 ◽  
Author(s):  
Darren Henry Brouwer ◽  
Sylvian Cadars ◽  
Kathryn Hotke ◽  
Jared Van Huizen ◽  
Nicholas Van Huizen

Structure determination of layered materials can present challenges for conventional diffraction methods due to the fact that such materials often lack full three-dimensional periodicity since adjacent layers may not stack in an orderly and regular fashion. In such cases, NMR crystallography strategies involving a combination of solid-state NMR spectroscopy, powder X-ray diffraction, and computational chemistry methods can often reveal structural details that cannot be acquired from diffraction alone. We present here the structure determination of a surfactant-templated layered silicate material that lacks full three-dimensional crystallinity using such an NMR crystallography approach. Through a combination of powder X-ray diffraction and advanced 29Si solid-state NMR spectroscopy, it is revealed that the structure of the silicate layer of this layered silicate material templated with cetyltrimethylammonium surfactant cations is isostructural with the silicate layer of a previously reported material referred to as ilerite, octosilicate, or RUB-18. High-field 1H NMR spectroscopy reveals differences between the materials in terms of the ordering of silanol groups on the surfaces of the layers, as well as the contents of the inter-layer space.


2013 ◽  
Vol 117 (23) ◽  
pp. 12258-12265 ◽  
Author(s):  
Dmytro V. Dudenko ◽  
P. Andrew Williams ◽  
Colan E. Hughes ◽  
Oleg N. Antzutkin ◽  
Sitaram P. Velaga ◽  
...  

2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Neil A. Williams ◽  
Mahboub Merzouk ◽  
Peter B. Hitchcock

A range of silver iminoalkyl imidazol-2-ylidene complexes have been isolated in good yield (50%–85%) and characterised by and NMR spectroscopy. A single crystal X-ray diffraction structure determination of 1--(benzylhydrylidene-amino)-ethyl-benzyl imidazol-2-ylidene silver bromide indicated monodentate coordination of the ligand.


1989 ◽  
Vol 44 (6) ◽  
pp. 659-665 ◽  
Author(s):  
Ulf Pindur ◽  
Ludwig Pfeuffer ◽  
Camran Flo ◽  
Werner Massa ◽  
Karin Seitz

The conformations of and charge distributions in indolyl(alkoxy)carbenium tetrafluoroborates 2, a new class of highly stabilized carbenium ions, were investigated by 1H and 13C NMR spectroscopy and the crystal structure of indol-3-yl(methoxy)phenylcarbenium tetrafluoroborate (2e) was determined by X-ray diffraction methods. The phenyl-substituted cation of 2e exhibits axial chirality in the crystalline state


2014 ◽  
Vol 92 (6) ◽  
pp. 542-548 ◽  
Author(s):  
Lucian-Cristian Pop ◽  
Nobuaki Kurokawa ◽  
Hiroaki Ebata ◽  
Katsuya Tomizawa ◽  
Tomoyuki Tajima ◽  
...  

The first stable stannanetriol and germanetriol bearing sterically congested aryl groups were synthesized by hydrolysis of the corresponding trichloro-stannane and -germane. The stannanetriol is monomeric in solution as well as in the crystalline state, as evidenced by X-ray diffraction analysis and CP-MAS NMR spectroscopy. The stannanetriol reacted with silicone grease to afford a cagelike compound having three Sn–O–Si–O–Sn linkages in the molecule. All the group 14 triols can be converted to the corresponding trihalo compounds in good yields.


2009 ◽  
Vol 64 (3) ◽  
pp. 343-346
Author(s):  
Michael Hagemann ◽  
Tania Pape ◽  
Norbert W. Mitzel

The reaction of lithium 2-(dimethylamino)ethanolate with Me2SiCl2 yielded a lithium chloride adduct of Me2Si- (OCH2CH2NMe2)2. Despite the application of an excess of Me2SiCl2, the formation of ClMe2SiOCH2CH2NMe2 was not observed. [Me2Si(OCH2CH2NMe2)2・Li2Cl2] was characterised by NMR spectroscopy and determination of its crystal structure by X-ray diffraction. In the solid state it forms endless chains consisting of Li2Cl2 rhombi, with the lithium atoms chelated by the O and N atom of one OCH2- CH2NMe2 substituent of Me2Si(OCH2CH2NMe2)2 units.


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