Synthesis and Structure of Pyrrolidinobromodiboranes(4)

2005 ◽  
Vol 60 (9) ◽  
pp. 1016-1019 ◽  
Author(s):  
Yong Nie ◽  
Hans Pritzkow ◽  
Walter Siebert
Keyword(s):  
Main Product ◽  
Molar Ratio ◽  
X Ray ◽  
New Compounds

The reaction of tetrapyrrolidinodiborane(4) (1) with BBr3 in a 1:1 molar ratio yields a mixture of 1,2-dibromo-1,2- dipyrrolidinodiborane(4) (2) and bromotripyrrolidino- diborane( 4) (3), while a 1:2 molar ratio leads in Et2O to compound 2 as the main product along with a small amount of [(C4H8N)2B2Br3(OEt)] (4). The new compounds have been characterized by NMR and MS data, as well as by X-ray structure analyses of 2 and 4, of which the former exhibits an interesting polymorphism phenomenon.

Reaktive E=C (p-p)π-Systeme, XL. / Reactive E=C(p-p)π Systems, XL.

1995 ◽  
Vol 50 (1) ◽  
pp. 94-100 ◽  
Author(s):  
Thomas Albers ◽  
Joseph Grobe ◽  
Duc Le Van ◽  
Bernt Krebs ◽  
Mechtild Läge
Keyword(s):  
Molecular Structure ◽  
Main Product ◽  
Chloroform Solution ◽  
Lone Pair ◽  
Secondary Amines ◽  
Molar Ratio ◽  
Electronic Interaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
New Compounds

The reaction of bis(trifluoromethyl)arsane 2 with secondary amines R2NH in a molar ratio of 1:3 at -60 °C allows the preparation of trifluoromethyl arsaalkenes of the type F3CAs=C(F)NR2 in moderate yields (15-35%) [NR2 = NMe2 (3a), NMeEt (3b), NEt2 (3c)]. The main product of the reaction of 2 with Me2NH is the 1,1-diamino compound F3CAs=C(NMe2)2 (4a). With ethyl(isopropyl)- or di(isopropyl)amine the corresponding derivatives F3CAs=C(F)NEt(iPr) (3d) and F3CAs=C(F)N(iPr)2 (3e), respectively, are formed only in traces (3d), or not at all (3 e). However, 3d and 3e can be prepared by reacting perfluoro-2-arsapropene with the corresponding secondary amines. The new compounds 3 a to 3 e can be stored at 20 °C in chloroform solution for hours without decomposition and show Z configuration without exception. The molecular structure of 1-(diethylamino)-1,3,3,3-tetrafluoro-2-arsapropene 3c, determined by an X-ray diffraction study on single crystals, indicates a strong electronic interaction of the lone pair on nitrogen with the AsC double bond. This results in a trigonal planar arrangement at the nitrogen atom, a strongly shortened sp2-CN-bond (1.312 Å), an elongated AsC distance (1.867 Å), and an almost planar skeleton of the molecule.

Synthese und Kristallstrukturen einiger Tetramethylstibonium-Hydrogendicarboxylate / Synthesis and Crystal Structures of Some Tetramethylstibonium Hydrogendicarboxylates

1982 ◽  
Vol 37 (11) ◽  
pp. 1393-1401 ◽  
Author(s):  
Beatrix Milewski-Mahrla ◽  
Hubert Schmidbaur
Keyword(s):  
Hydrogen Bonds ◽  
Crystal Structures ◽  
Spectroscopic Data ◽  
Molar Ratio ◽  
Ionic Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carboxylate Oxygen ◽  
Donor Acceptor ◽  
New Compounds

Reactions of pentamethylantimony (CH3)5Sb with carboxylic acids in the molar ratio 1:2 afford one equivalent of methane and essentially quantitative yields of crystalline tetramothylstibonium hydrogendicarboxylates. Six new compounds of this series have been synthesized using benzoic, o-phthalic, salicylic, 4-ethoxy-salicylic, oxalic, and malic acid, and characterized by analytical and spectroscopic data. An ionic structure with strong hydrogen bonds in the anionic components is proposed.The crystal structures of the hydrogen-dibenzoato (1), hydrogen-ortho-plithalato (2) and 4-ethoxy-hydrogen-salicylate (3) were determined by single crystal X-ray diffraction. The compounds can be described as having ionic lattices with some donor-acceptor inter­actions between the stibonium centers and the carboxylate oxygen atoms. The anions are characterized by strong hydrogen bonds O...H...O. Thus, the (CH3)4Sb-tetrahedron in 1 is distorted by two benzoate oxygon atoms (at 304(2) and 340(2) pin). The cation in 2 is largely undistorted and the anion has a hydrogenphthalate hydrogen bond of d(O...H...O) = 232 pm. The cation-anion contact in 3 is as short as d(Sb-O) = 289 pm rendering the Sb atom pentacoordinate.

Zwei neue Bis(trimethylsilyl)aminoderivate des Antimons: MeSb(N{SiMe3}2)2 und MeCl2Sb(N{SiMe3}2)2

1985 ◽  
Vol 40 (7) ◽  
pp. 872-877 ◽  
Author(s):  
W. Kolondra ◽  
W. Schwarz ◽  
J. Weidlein
Keyword(s):  
Raman Spectra ◽  
Structure Determination ◽  
Ir And Raman Spectra ◽  
Molar Ratio ◽  
Monoclinic Space Group ◽  
Space Group ◽  
X Ray ◽  
R Value ◽  
New Compounds ◽  
Ir And Raman

Abstract Unexpectedly the reaction of SbCl3 with Na(N{SiMe3}2) in a 1:3 molar ratio forms MeSb(N{SiMe3}2)2, I, (Me = CH3) and other trimethylsilyl compounds. The colourless and liquid methylstibane derivative I is monomeric in solution and forms MeSbCl2(N{SiMe3}2)2 (II) on reaction with SO2Cl2. Both new compounds have been characterized by analyses, NMR, IR and Raman spectra. The X-ray structure determination for II shows the monoclinic space group P21/C with 4 monomeric units per cell. The structure was refined to an R-value of 0,052.

Synthesis and structural characterization of zinc complexes of the imido–amido phosphate anions OP[(NHR)3–x(NR)]x– (R = Me, t-Bu; x = 1–3) and EP[(NH-t-Bu)2(N-t-Bu)]– (E = S, NSiMe3)

2005 ◽  
Vol 83 (10) ◽  
pp. 1768-1778 ◽  
Author(s):  
Andrea F Armstrong ◽  
Tristram Chivers ◽  
Mark Krahn ◽  
Masood Parvez
Keyword(s):  
Nmr Spectroscopy ◽  
Structural Characterization ◽  
Zinc Phosphate ◽  
Membered Ring ◽  
Molar Ratio ◽  
Centrosymmetric Dimer ◽  
X Ray ◽  
Phosphate Anions ◽  
New Compounds

The reaction of OP(NH-t-Bu)3 with 1 equiv. of ZnMe2 generates the dimeric eight-membered ring {MeZn[(µ-NH-t-Bu)(µ-N-t-Bu)P(NH-t-Bu)(µ-O)]}2 (5) and the cubane {[MeZn]3[OP(N-t-Bu)3][OP(NH-t-Bu)3]} (6), which contains the first known trisimidophosphate trianion. A related complex {Zn[ZnMe]2[OP(N-t-Bu)(NH-t-Bu)2][OP(N-t-Bu)3]} (7) is obtained by the reaction of OP(NH-t-Bu)3 with ZnMe2 in a 2:3 molar ratio. The treatment of OP(NHMe)3 with 1 equiv. of ZnMe2 produces the oxide-templated cluster {Zn4(µ4-O)[OP(NMe)(NHMe)2]4[OP(NMe)2(NHMe)]}2 (8). Each half of this centrosymmetric dimer contains a tetrahedral arrangement of four 4-coordinate Zn2+ ions surrounding the central µ4-O2- anion. The reaction of SP(NH-t-Bu)3 with ZnMe2 in a 1:1 molar ratio generates the dimer {MeZn(µ-S)(µ-N-t-Bu)P(NH-t-Bu)2}2 (10), which has a ladder-type structure. When a 2:1 molar ratio of the same reagents is employed, the bis(N,S)-chelated complex {Zn[(µ-S)(µ-N-t-Bu)P(NH-t-Bu)2]2} (11) is obtained. The monomeric N,N′-chelated complex {MeZn[(µ-N-t-Bu)(µ-NSiMe3)P(NH-t-Bu)2]} (12) results from the reaction of Me3SiNP(NH-t-Bu)3 with 1 equiv. of dimethylzinc. All new compounds have been characterized by multinuclear (1H, 13C, and 31P) NMR spectroscopy and, in the case of 5, 6, 7, 8, and 10, by X-ray structural determinations.Key words: zinc, phosphate, imido ligands, sulfur.

AlkalineEarthMetal-Hydride-Iodide Compounds: Syntheses andCrystal Structures of Sr2H3I and Ba5H2I3.9(2)O2

2011 ◽  
Vol 66 (1) ◽  
pp. 21-26
Author(s):  
Olaf Reckeweg ◽  
Francis J. DiSalvo
Keyword(s):  
Single Crystal ◽  
Single Crystals ◽  
Structural Model ◽  
Structure Type ◽  
Lattice Parameters ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
New Compounds

Single crystals of Sr2H3I andBa5H2I3.9(2)O2 were obtained by reacting Sr or Ba, respectively, with dried and sublimed NH4I in a 4 : 1 molar ratio in silica-jacketed Nb ampoules for 13 h at 1200 K. The crystal structures of the new compounds have been determined by means of single-crystal X-ray diffraction. Sr2H3I crystallizes in a stuffed anti-CdI2 structure isotypic to Ba2H3Cl in the space group P3m1 (no. 164) with the lattice parameters a = 426.0(1) and c = 774.9(2) pm, while Ba5H2I3.9(2)O2 crystallizes in a new structure type in the space group Cmcm (no. 63) with the lattice parameters a = 1721.0(2), b = 1452.5(2) and c = 639.03(9) pm. The structural results for Sr2H3I are corroborated by EUTAX calculations. For the disordered compound Ba5H2I3.9(2)O2, EUTAX calculations on an approximated, ordered structural model were used to find possible insights into the disorder

Über die Darstellung und Eigenschaften neuer Chloro-tris(carbonylmetaIIato)-zinn(IV)-Komplexe und die Kristallstruktur von ClSn[Fe(CO)2Cp]2[Co(CO)4]. Synthesis and Properties of New Chloro Tris(carbonylmetalato) Tin(IV) Complexes and the X-ray Structure Analysis of ClSn[Fe(CO)2Cp]2[Co(CO)4]

1980 ◽  
Vol 35 (9) ◽  
pp. 1115-1124 ◽  
Author(s):  
Matthias Moll ◽  
Helmut Behrens ◽  
Peter Merbach ◽  
Klaus Görting ◽  
Günter Liehr ◽  
...  
Keyword(s):  
Structure Analysis ◽  
Molar Ratio ◽  
Space Group ◽  
X Ray ◽  
New Compounds ◽  
Fir Spectra

The chloro-tris(carbonylmetalato)tin(IV) compounds, listed in Table I, are obtained by the reaction of TlCo(CO)4 or Tl[Mn(CO)5]3 with the dichloro(carbonylmetalato)tin(IV) complexes Cl2Sn[M(CO)5]2 (M = Mn, Re), Cl2Sn[Fe(CO)2Cp]2, Cl2Sn[Cr(CO)3Cp][Mn(CO)5] and Cl2Sn[Cr(CO)3Cp][Fe(CO)2Cp] in the molar ratio 1:1. Chloro-tris(carbonylmetalato)- tin(TV) compounds of the same type are also formed by treatment of TlCo(CO)4 with the trichloro(carbonylmetalato)tin(IV) complexes in the molar ratio 2 : 1. The new compounds are characterized by their analyses, mass, IR and FIR spectra. The X-ray analysis of ClSn[Fe(CO)2Cp]2[Co(CO)4] (space group P21/c) confirms the presence of 3 carbonyl - metalato groups attached to tin.

Effect of Hydrated Metal Salts on the Coordination Product of Cobalt(II) halide and PNP Type Ligand, 2,6-bis(di-tertbutylphosphinomethyl) pyridine

2018 ◽  
Author(s):  
Tasneem Siddiquee ◽  
Abdul Goni
Keyword(s):  
Metal Salts ◽  
Molar Ratio ◽  
Pincer Complexes ◽  
Asymmetric Unit ◽  
X Ray Diffraction ◽  
Pincer Ligand ◽  
Tetrahedral Geometry ◽  
X Ray ◽  
Distorted Tetrahedral Geometry ◽  
Cobalt Center

Chemical treatment of CoX<sub>2</sub><b><sup>. </sup></b>6H<sub>2</sub>O (X = Cl, Br, I) with the potentially tridentate PNP pincer ligand 2,6-bis(di-<i>tert</i>-butylphosphinomethyl)pyridine in 1:1 molar ratio results in cobalt(II) halide-PNP pincer complexes. The effect of the hydrated metal source on molecular structure and geometry of the complexes was studied by single crystal X-ray diffraction analysis. The complexes are neutral and the cobalt center adopts a penta-coordinate system with potential atropisomerization. Within the unit cell there are two distinct molecules per asymmetric unit. One of the two phosphorus atoms in the PNP ligand was observed to be partially oxidized to phosphinoxide. Disorder in the structure reflects a mixture of square pyramidal and distorted tetrahedral geometry.

scholarly journals Photocatalytic Reduction of CO2 to Methanol Using a Copper-Zirconia Imidazolate Framework

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 346
Author(s):  
Sonam Goyal ◽  
Maizatul Shima Shaharun ◽  
Ganaga Suriya Jayabal ◽  
Chong Fai Kait ◽  
Bawadi Abdullah ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalyst Support ◽  
Oxidation Potential ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Optimum Parameters ◽  
Reduction Of Co2 ◽  
Enhanced Yield

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.

scholarly journals Fusarins G–L with Inhibition of NO in RAW264.7 from Marine-Derived Fungus Fusarium solani 7227

Marine Drugs ◽  
2021 ◽  
Vol 19 (6) ◽  
pp. 305
Author(s):  
Guangyuan Luo ◽  
Li Zheng ◽  
Qilin Wu ◽  
Senhua Chen ◽  
Jing Li ◽  
...  
Keyword(s):  
Fusarium Solani ◽  
2D Nmr ◽  
Inflammatory Activity ◽  
Raw264.7 Cells ◽  
Spectroscopic Methods ◽  
X Ray ◽  
X Ray Crystallography ◽  
Structure Activity ◽  
Ic50 Values ◽  
New Compounds

Six new fusarin derivatives, fusarins G–L (1–6), together with five known compounds (5–11) were isolated from the marine-derived fungus Fusarium solani 7227. The structures of the new compounds were elucidated by means of comprehensive spectroscopic methods (1D and 2D NMR, HRESIMS, ECD, and ORC) and X-ray crystallography. Compounds 5–11 exhibited potent anti-inflammatory activity by inhibiting the production of NO in RAW264.7 cells activated by lipopolysaccharide, with IC50 values ranging from 3.6 to 32.2 μM. The structure–activity relationships of the fusarins are discussed herein.

scholarly journals 4-vinylpyridine derivatives: Protonation, methylation and silver(I) coordination chemistry

2021 ◽  
pp. 174751982198965
Author(s):  
Guoqi Zhang
Keyword(s):  
Mass Spectrometry ◽  
Schiff Base ◽  
Coordination Chemistry ◽  
Elemental Analysis ◽  
Silver Complex ◽  
Spectroscopic Techniques ◽  
X Ray ◽  
X Ray Crystallography ◽  
Pyridine Moiety ◽  
New Compounds

( E)-4-[2-(Pyridin-4-yl)vinyl]benzaldehyde, containing both a 4-vinylpyridine and an aldehyde functionality, is utilized to develop new, highly conjugated chalcone compounds and a bis-Schiff base azine compound. The chalcone-containing compounds are further explored for their protonation, methylation and silver(I) coordination chemistry using the pyridine moiety. In parallel, a cyano-containing analogue, ( E)-4-[2-(pyridin-4-yl)vinyl]benzonitrile is also synthesized and studied for its silver(I) coordination chemistry. These new compounds are fully characterized by mass spectrometry, elemental analysis and spectroscopic techniques. The methylated product of ( E)-1-(9-anthryl)-3-{4-[2-(pyridin-4-yl)vinyl]phenyl}prop-2-en-1-one and a silver complex of ( E)-4-[2-(pyridin-4-yl)vinyl]benzonitrile are structurally determined by X-ray crystallography.

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