Novel ditopic receptors based on the P2N2 diphosphazane ring: synthesis and x-ray structural characterization of cis and trans bis(crown ether) annelated 1,3,2.lambda.5,4.lambda.5-diazadiphosphetidine 2,4-disulfide

1989 ◽  
Vol 111 (18) ◽  
pp. 7136-7144 ◽  
Author(s):  
Jean Pierre Dutasta ◽  
Jean Paul Declercq ◽  
Carmen Esteban-Calderon ◽  
Bernard Tinant

2018 ◽  
Vol 96 (6) ◽  
pp. 570-577 ◽  
Author(s):  
Alina M. Secara ◽  
Justin F. Binder ◽  
Ala’aeddeen Swidan ◽  
Charles L.B. Macdonald

A series of germanium(II) and tin(II) bromide polyether complexes have been synthesized. Specifically, [GeBr([15]crown-5)][GeBr3], [GeBr([18]crown-6)][GeBr3], [GeBr(triglyme)][GeBr3], [GeBr(tetraglyme)][GeBr3], [SnBr([18]crown-6)][SnBr3], [Sn([15]crown-5)2][SnBr3]2, [SnBr(triglyme)][SnBr3], and [SnBr(tetraglyme)][SnBr3] have been fully characterized including by single crystal X-ray diffraction. The synthesis of [GeBr(dibenzo[24]crown-8)][GeBr3] and [GeCl(dibenzo[24]crown-8)][GeCl3] are also reported, along with the crystal structure of the latter’s water adduct, which features a water molecule adjacent to the GeCl+ ion within the cavity of the crown ether.



2011 ◽  
Vol 8 (s1) ◽  
pp. S323-S329
Author(s):  
Shahriare Ghammamy ◽  
Hajar Sahebalzamani

The crystal structure of [(CH3)4N]4[WOCl4F][WO3Cl4] was determined by single crystal x-ray diffraction technique. The crystal is monoclinic, space group C 2/m, with a= 28.23(10) Å, b= 11.60(4) Å,c= 13.48(5) Å, β=118.43(7)°, V= 3886(2)Å3, Z=4. The structure was solved by direct methods and refined by least-squares methods to a final R = 0.0512 for 3825 observed reflections with I>2σ(I). In crystal there are two crystallographic distinct anions, both with cis geometry; the O-W-F and O-W-O angles are 97.5(3)° and 103.1(3) ° respectively. All structures are cis configurations that confirm a preference for angles below 90° and 180° between cis and trans σ-donor ligands, respectively.



2007 ◽  
Vol 2007 (suppl_26) ◽  
pp. 61-66 ◽  
Author(s):  
B. Peplinski ◽  
B. Adamczyk ◽  
G. Kley ◽  
K. Adam ◽  
F. Emmerling ◽  
...  


Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.



1988 ◽  
Vol 6 (3) ◽  
pp. 1946-1949 ◽  
Author(s):  
B. T. Jonker ◽  
S. B. Qadri ◽  
J. J. Krebs ◽  
G. A. Prinz


2005 ◽  
Vol 66 (1) ◽  
pp. 81-90 ◽  
Author(s):  
A. Erenburg ◽  
E. Gartstein ◽  
M. Landau


2012 ◽  
Vol 16 (01) ◽  
pp. 154-162 ◽  
Author(s):  
Edwin W.Y. Wong ◽  
Daniel B. Leznoff

The reduction of magnesium phthalocyanine (MgPc) with 2.2 equivalents of potassium graphite in 1,2-dimethoxyethane (DME) gives [K2(DME)4]PcMg(OH)(1) in 67% yield. Compound 1 was structurally characterized using single crystal X-ray crystallography and was found to be a monomeric, heterometallic complex consisting of a μ3-OH ligand that bridges a [MgIIPc3-]- anion to two potassium cations solvated by four DME molecules. An absorption spectrum of 1 confirms the Pc ligand is singly reduced and has a 3–charge. The solid-state structure of 1 does not indicate breaking of the aromaticity of the Pc ligand. Compound 1 is only the second Pc3- complex and the first reduced MgPc to be isolated and structurally characterized.





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