Anionic indabenzene: synthesis and characterization

2017 ◽  
Vol 53 (99) ◽  
pp. 13260-13263 ◽  
Author(s):  
Taichi Nakamura ◽  
Katsunori Suzuki ◽  
Makoto Yamashita
Keyword(s):  
Nmr Spectroscopy ◽  
Synthesis And Characterization ◽  
X Ray ◽  
Multinuclear Nmr ◽  
X Ray Crystallography ◽  
Multinuclear Nmr Spectroscopy

An anionic indabenzene was synthesized via the transmetallation of an aluminacyclohexadiene with bulky silyl substituents, and fully characterized using multinuclear NMR spectroscopy and X-ray crystallography.

Consecutive N2 loss from a uranium diphosphazide complex

2020 ◽  
Vol 49 (3) ◽  
pp. 578-582 ◽  
Author(s):  
Tara K. K. Dickie ◽  
Connor S. MacNeil ◽  
Paul G. Hayes
Keyword(s):  
Nmr Spectroscopy ◽  
X Ray ◽  
Multinuclear Nmr ◽  
X Ray Crystallography ◽  
Multinuclear Nmr Spectroscopy ◽  
Uranium Species

A uranium(iv) complex supported by an unusual diphosphazide ligand was prepared. Controlled, consecutive N2 loss was observed, affording well-defined uranium species that were characterized by multinuclear NMR spectroscopy and X-ray crystallography.

Synthesis and Reactivity of Novel Alkali Metal Stannides

2004 ◽  
Vol 59 (11-12) ◽  
pp. 1462-1470 ◽  
Author(s):  
Thorsten Schollmeier ◽  
Ulrich Englich ◽  
Roland Fischer ◽  
Ingo Prass ◽  
Karin Ruhlandt ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Alkali Metal ◽  
Synthesis And Characterization ◽  
Metal Compounds ◽  
X Ray ◽  
X Ray Crystallography ◽  
Multinuclear Nmr Spectroscopy ◽  
Alkali Metal Compounds ◽  
Potassium Hydride

Reactivity and side products of reactions of diorganodihydridostannanes (R2SnH2, R = Me, nBu, tBu)) with various alkali metal compounds have been discussed. Alternatively, the synthesis and characterization of a family of novel potassium stannides are described as well. The compounds of type (RR’2Si)R”2SnK (R, R’= Me, Ph; R”= , Me, tBu, Ph) 4 - 9 were synthesized by reaction of potassium hydride with bis(silyl)stannides ((RR’2Si)2SnR”2). All compounds were characterized by multinuclear NMR spectroscopy. In addition, the tri-tert-butyltin compound 3 (LiSntBu3) and the unsymmetrical silyl substituted stannane 10 were characterized by X-ray crystallography.

Pentafluorophenyl and phenyl substituted azidoborates

2002 ◽  
Vol 80 (11) ◽  
pp. 1444-1450 ◽  
Author(s):  
Wolfgang Fraenk ◽  
Thomas M Klapötke ◽  
Burkhard Krumm ◽  
Heinrich Nöth ◽  
Max Suter ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Single Crystal ◽  
Boron Atom ◽  
Single Crystal Diffraction ◽  
X Ray ◽  
Multinuclear Nmr ◽  
X Ray Crystallography ◽  
Multinuclear Nmr Spectroscopy

The azidoborates [(C6F5)4–nB(N3)n]– (n = 1–3) (1–3) were synthesized by reacting the corresponding borane with [R]N3 (R = Me4N, Ph4P). To study the influence of the electron withdrawing C6F5-substituent on the boron atom, [Me4N][(C6H5)3BN3] (4) was also prepared. All compounds were fully characterized by IR, Raman, and multinuclear NMR spectroscopy in addition to characterization by single crystal diffraction analyses.Key words: azidoborate, pentafluorophenyl, multinuclear NMR spectroscopy, X-ray crystallography.

scholarly journals Exocyclic Enamines of Pyrrolo[1,2-a]quinoxalines Generated by 1,3-dipolar Cycloaddition Reactions of Benzimidazolium Ylides to Activated Alkynes

2001 ◽  
Vol 71 (3) ◽  
pp. 197-209 ◽  
Author(s):  
Alina Nicolescu ◽  
Emilian Georgescu ◽  
Florea Dumitrascu ◽  
Florentina Georgescu ◽  
Florina Teodorescu ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Dipolar Cycloaddition ◽  
Cycloaddition Reactions ◽  
X Ray ◽  
Multinuclear Nmr ◽  
X Ray Crystallography ◽  
Mild Conditions ◽  
Quinoxaline Derivatives ◽  
Multinuclear Nmr Spectroscopy ◽  
Activated Alkynes

The reactions of N-acetonylbenzimidazolium chlorides with various activated alkynes, in the presence of bases, led under mild conditions to a mixture of pyrrolo[1,2-a]benzimidazoles (3), 4-methylene-pyrrolo[1,2-a]quinoxaline derivatives (4) and pyrrolo[1,2-a]quinoxalin-4-one derivatives (5). The exocyclic enamine derivatives 4 have been fully characterized by multinuclear NMR spectroscopy and X-ray crystallography. A mechanism rationalizing the formation of the enamine derivatives is proposed.

Solid-State Structure and Tautomerism of 2-Aminotroponimines Studied by X-ray Crystallography and Multinuclear NMR Spectroscopy

2004 ◽  
Vol 2004 (21) ◽  
pp. 4452-4466 ◽  
Author(s):  
Rosa M. Claramunt ◽  
Dionisia Sanz ◽  
Marta Pérez-Torralba ◽  
Elena Pinilla ◽  
M. Rosario Torres ◽  
...  
Keyword(s):  
Solid State ◽  
Nmr Spectroscopy ◽  
State Structure ◽  
Solid State Structure ◽  
X Ray ◽  
Multinuclear Nmr ◽  
X Ray Crystallography ◽  
Multinuclear Nmr Spectroscopy
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