π-Olefin-Iridium-Komplexe, XIII [1] Neuartige metallzentrierte Verknüpfung zweier Tolan-Moleküle / π-Olefin Iridium Complexes, XIII [1] Novel Metal-Centered Linkage of Two Tolane Molecules

1986 ◽  
Vol 41 (1) ◽  
pp. 76-78 ◽  
Author(s):  
Jörn Müller ◽  
Matthias Tschampel ◽  
Joachim Pickardt
Keyword(s):  
Diffraction Analysis ◽  
Spectroscopic Methods ◽  
Iridium Complexes ◽  
X Ray Diffraction ◽  
Methyl Group ◽  
X Ray

Reaction of [(cod)IrI]2 (cod = 1,5-cyclooctadiene) with methyllithium in the presence of diphenylacetylene (tolane) yields a (cod)Ir complex (3) with a 1-benzyl-2.3-diphenyl-7-methyl-indenyl ligand which is formed by a novel cyclization of two tolane units with participation of a methyl group. The compound was characterized by spectroscopic methods and by X-ray diffraction analysis.

Bis(μ-carboxylato)dienerhodium(I) Complexes - Synthesis, Characterization and Catalytic Activity

2008 ◽  
Vol 73 (8-9) ◽  
pp. 1205-1221 ◽  
Author(s):  
Jiří Zedník ◽  
Jan Sedláček ◽  
Jan Svoboda ◽  
Jiří Vohlídal ◽  
Dmitrij Bondarev ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Diffraction Analysis ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray

Dinuclear rhodium(I) η2:η2-cycloocta-1,5-diene (series a) and η2:η2-norborna-2,5-diene (series b) complexes with μ-RCOO- ligands, where R is linear C21H43 (complexes 1a, 1b), CH2CMe3 (2a, 2b), 1-adamantyl (3a, 3b) and benzyl (4a, 4b), have been prepared and characterized by spectroscopic methods. Structures of complexes 2b, 3a and 4a were determined by X-ray diffraction analysis. Complexes prepared show low to moderate catalytic activity in polymerization of phenylacetylene in THF giving high-cis-transoid polymers, but they show only oligomerization activity in dichloromethane.

scholarly journals A Pair of New Polyketide Enantiomers from Three Endolichenic Fungal Strains Nigrospora sphaerica, Alternaria alternata, and Phialophora sp

2016 ◽  
Vol 11 (6) ◽  
pp. 1934578X1601100 ◽  
Author(s):  
Jun-Wei He ◽  
Chuan-Xi Wang ◽  
Li Yang ◽  
Guo-Dong Chen ◽  
Dan Hu ◽  
...  
Keyword(s):  
Diffraction Analysis ◽  
Alternaria Alternata ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fungal Strains ◽  
The Absolute ◽  
Modified Mosher’S Method

A pair of new enantiomeric polyketides, (-)- and (+)-nigrosporaol A (1a and 1b), along with one related known compound, (±)-alternarienoic acid (2), were isolated from three endolichenic fungal strains, Nigrospora sphaerica (No.83-1-1-2), Alternaria alternata (No.58-8-4-1), and Phialophora sp.(No.96-1-8-1). Their structures, including the absolute configurations, were elucidated on the basis of spectroscopic methods, X-ray diffraction analysis, and the modified Mosher's method.

π-Olefin-Iridium-Komplexe, XXII [1]. C-H-Aktivierung von aromatischen und aliphatischen Solvensmolekülen RH bei der Reaktion von [Cp*IrCI2]2 mit Butadienmagnesium unter Bildung von [Cp*Ir(η3-C4H7)R] sowie Kristallstruktur von [Cp*Ir(η3-C4H7)C6H5] / π-Olefin Iridium Complexes, XXII [1]. C-H Activation of Aromatic and Aliphatic Solvent Molecules RH in the Reaction of [Cp*IrCl2]2 with Butadienemagnesium with Formation of [Cp*Ir(η3-C4H7)R], and Crystal Structure of [Cp*Ir(η3-C4H7)C6H5]

1994 ◽  
Vol 49 (12) ◽  
pp. 1645-1653 ◽  
Author(s):  
Jörn Müller ◽  
Petra Escarpa Gaede ◽  
Ke Qiao
Keyword(s):  
Crystal Structure ◽  
Low Temperature ◽  
Diffraction Analysis ◽  
Iridium Complexes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nmr Spectrometry ◽  
Benzene Toluene ◽  
Solvent Molecules ◽  
Mechanism Of The Reaction

Reactions of [Cp*IrCl2]2 (Cp*=η3-C5Me5) with [MgC4H6·2 THF]n at low temperature give [Cp*Ir(η4-C4H6)] together with [Cp*Ir(η3-C4H7)R] compounds, the latter being formed via C-H activation of solvent molecules RH (RH = benzene, toluene, anisole, thiophene, furane, N-methylpyrrole, pentane, cyclohexane. THF). In the case of pyrrole, C-N -activation occurs. The ratio of syn and anti isomers of the 1-methylallyl complexes as well as the sites of C-H activation of RH were investigated by NMR spectrometry. An enantiomorphous crystal of [Cp*Ir(η3-C4H7)C6Hs] was characterized by X-ray diffraction analysis which reveals trigonal planar coordination at the Ir atom and an exo, syn conformation of the 1-methylallyl ligand. A mechanism of the reaction which involves 16-electron intermediates is discussed. The corresponding system [Cp*RhCl2]2/butadienemagnesium/RH gives only [Cp*Rh(η4-C4H6)], and no C-H activation is observed.

scholarly journals Jatroidaine A: a New Tetranortirucallane Type Triterpene from Jatropha multifida

2021 ◽  
Vol 15 (5) ◽  
pp. 408-413
Author(s):  
Fei Li ◽  
Liang Ma ◽  
Jinyuan Zhang ◽  
Xueling Qiao ◽  
Dingshan Zhang ◽  
...  
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Absolute Configuration ◽  
Thioredoxin Reductase ◽  
Spectroscopic Methods ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inhibitory Activities ◽  
Jatropha Multifida

Jatroidaine A (1), a new tetranortirucallane-type triterpene, and two known analogues (2−3) were isolated from the leaves and branches of Jatropha multifida. Their structures were fully elucidated by extensive spectroscopic methods and comparison to known compounds. The absolute configuration of 1 was assigned by single-crystal X-ray diffraction analysis. All compounds were evaluated for their anti-inflammatory and thioredoxin reductase (TrxR) inhibitory activities. Unfortunately, no significant activity was observed.

Large interaction energy for the homodimer and the heterodimer extracted from the supramolecular chain of a bent trinuclear zinc(II) complex with a reduced Schiff base ligand

2022 ◽  
Author(s):  
Mainak Karmakar ◽  
Rosa M. Gomila ◽  
Antonio Frontera ◽  
Shouvik Chattopadhyay
Keyword(s):  
Schiff Base ◽  
Diffraction Analysis ◽  
Schiff Base Ligand ◽  
Zinc Complex ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
Amino Groups ◽  
X Ray ◽  
Reduced Schiff Base ◽  
Large Interaction

A bent trinuclear zinc complex, [Zn{ZnIL}2]•DMF {H2L = 2,2'-[(2,2-Dimethyl-1,3-propanediyl)bis(iminomethylene)]bis[6-methoxyphenol]} was synthesized and characterized by standard spectroscopic methods and X-ray diffraction analysis. The existence of coordinated amino groups and iodide counter...

Bis/tris[octakis(hexylthio)phthalocyaninato] europium(III) complexes: structure, spectroscopic, and electrochemical properties

2013 ◽  
Vol 17 (08n09) ◽  
pp. 673-681 ◽  
Author(s):  
Chunhua Huang ◽  
Yi Zhang ◽  
Junshan Sun ◽  
Yongzhong Bian ◽  
Dennis P. Arnold
Keyword(s):  
Cyclic Voltammetry ◽  
Ir Spectroscopy ◽  
Diffraction Analysis ◽  
Electrochemical Properties ◽  
Electronic Absorption ◽  
Elemental Analysis ◽  
Molecular Structures ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray

Bis/tris(phthalocyaninato) europium double- and triple-decker complexes Eu [ Pc (β- SC 6 H 13)8]2 (1) and Eu 2[ Pc (β- SC 6 H 13)8]3 (2) [ Pc (β- SC 6 H 13)8 = 2, 3, 9, 10, 16, 17, 23, 24-octakis(hexylthio)phthalocyaninate] have been synthesized and characterized by a series of spectroscopic methods including mass, NMR, electronic absorption and IR spectroscopy in addition to elemental analysis. Their molecular structures have been determined by single crystal X-ray diffraction analysis and electrochemical properties studied by cyclic voltammetry.

scholarly journals 5α,8α-Epidioxysterols from a Formosan Sponge, Axinyssa sp

2013 ◽  
Vol 8 (11) ◽  
pp. 1934578X1300801
Author(s):  
Tzu-Rong Su ◽  
Kai-Ju Liang ◽  
Michael Y. Chiang ◽  
Mei-Chin Lu ◽  
Yu-Jen Wu ◽  
...  
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Cell Lines ◽  
Cancer Cell ◽  
Absolute Configuration ◽  
Cancer Cell Lines ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Time

One new 5α,8α-epidioxysterol, 3-acetylaxinysterol (1), along with one known sterol, axinysterol (2), were isolated from a Formosan sponge, Axinyssa sp.. The structures of the compounds were determined by spectroscopic methods and the absolute configuration of 2 was further confirmed by single-crystal X-ray diffraction analysis for the first time. Compound 2 exhibited significant cytotoxicity against K562 and Molt 4 cancer cell lines.

Epoxy-trans-isodihydrorhodophytin, ein neuer Metabolit aus Laurencia obtusa / Epoxy-trans-isodihydrorhodophytin, a New Metabolit from Laurencia obtusa

1987 ◽  
Vol 42 (5) ◽  
pp. 507-509 ◽  
Author(s):  
Sedat Imre ◽  
Hermann Lotter ◽  
Hildebert Wagner ◽  
Ronald H. Thomson
Keyword(s):  
Diffraction Analysis ◽  
Red Algae ◽  
Spectroscopic Methods ◽  
Marmara Sea ◽  
X Ray Diffraction ◽  
X Ray

Abstract Laurencia obtusa, Red Algae, Rhodomelaceae, Acetylenic Ether Epoxy-trans-isodihydrorhodophytin, a new halogenated acetylenic bicyclic ether, has been isolated from a Laurencia obtusa variety, collected in the Marmara sea. Its structure was determined by spectroscopic methods and X-ray diffraction analysis.

scholarly journals Palladium(II) complexes with R2edda derived ligands, Part I: Reaction of diisopropyl (S,S)-2,2'-(1,2-ethanediyldiimino)- dipropanoate with K2[PdCl4]

2009 ◽  
Vol 74 (4) ◽  
pp. 389-400 ◽  
Author(s):  
Bojana Krajcinovic ◽  
Goran Kaludjerovic ◽  
Dirk Steinborn ◽  
Harry Schmidt ◽  
Christoph Wagner ◽  
...  
Keyword(s):  
Dft Calculations ◽  
Diffraction Analysis ◽  
13C Nmr ◽  
Ester Group ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
1H And 13C Nmr ◽  
X Ray

The reaction of K2[PdCl4] with (S,S)-(i-Pr)2eddip diester (diisopropyl (S,S)-2,2'-(1,2-ethanediyldiimino)dipropanoate) resulted in {PdCl2[(S,S)-(i- -Pr)2eddip-?2N,N']} (1) and {PdCl[(S,S)-(i-Pr)eddip-?2N,N',?O]} (2) with one hydrolyzed ester group. The compounds were characterized by spectroscopic methods and it was proved that the reaction is diastereoselective (1H- and 13C-NMR) in the case of 2 (one diastereoisomer of four possible). The structure of 2 was determined by X-ray diffraction analysis, indicating that the product is the (R,R)-N,N' configured isomer. In contrast, the reaction yielding 1 produced two of three possible diastereoisomers. DFT calculations support the formation of two diastereoisomers of 1 and of one diastereoisomer of 2.

Bis(trimethylphosphan)-η5-cyclopentadienyl- tert- butylimidovanadium( III): Reaktionen mit Schwefel, Selen, Tellur und Iod

2003 ◽  
Vol 58 (4) ◽  
pp. 237-245 ◽  
Author(s):  
Martin Billen ◽  
Gabriele Hornung ◽  
Gotthelf Wolmershäuser ◽  
Fritz Preuss
Keyword(s):  
Single Crystal ◽  
Diffraction Analysis ◽  
Spectroscopic Methods ◽  
X Ray Diffraction ◽  
X Ray

The reaction of [tBuN=VCp(PMe3)2] (1) with S8, Se, Te or I2 have been studied. Via this pathway dinuclear diamagnetic tert-butylimidovanadium(IV) complexes are formed: [(μ-E)(μ- NtBu)2V2Cp2] (E=S, Se, Te), [(μ-η1−E2)(μ-NtBu)2V2Cp2] {E=Se (3), Te}, [(μ-NtBu)2V2Cp2I2]. In addition the vanadium(V) complexes [tBuN=VCp (S5)] (9a) and tBuN=VCpI2 could be isolated. The synthesis of tBuN=VCpF2 is also described. All compounds obtained have been characterized by spectroscopic methods (MS; 1H, 13C, 51V NMR), 3 and 9b by single crystal X-ray diffraction analysis.

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