In the complexes [Ni(cyclam)(OCOR)2] (cyclam = 1,4,8,11-tetraazacyclotetradecane), where (RCOO)- is 2-naphthoate [bis-(2-naphthoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (I), monoclinic P2(1)/c, Z' = 0.5], 3,5-dinitrobenzoate [bis-(3,5-dinitrobenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (II), triclinic P1, Z' = 0.5], 4-nitrobenzoate [bis-(4-nitrobenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (III), monoclinic P2(1)/n, Z' = 0.5], 3-hydroxybenzoate [bis-(3-hydroxybenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (IV), monoclinic P2(1)/c, Z' = 0.5] and 4-aminobenzoate [bis-(4-aminobenzoato)-1,4,8,11-tetraazacyclotetradecanenickel(II), (V), monoclinic C2/c, Z' = 0.5], the Ni lies on a centre of inversion with monodentate carboxylato ligands occupying trans sites. Compound (I) consists of isolated molecules. In (II) and (III), N-H...O hydrogen bonds link the complexes into chains. Compounds (IV) and (III) form two- and three-dimensional structures generated entirely by hard hydrogen bonds. The 5-hydroxyisophthalate(2-) anion forms a hydrated complex, [Ni(cyclam)(5-hydroxyisophthalate)(H2O)]*4H2O [[aqua-(5-hydroxyisophthalato)-1,4,8,11-tetraazacyclotetradecanenickel(II)] tetrahydrate, (VI), monoclinic Cc, Z' = 1], in which the monodentate carboxylato ligand and a water molecule occupy trans sites at Ni: extensive hydrogen bonding links the molecular aggregates into a three-dimensional framework. The terephthalate(2-) anion forms a hydrated linear coordination polymer [catena-poly[terephthalato-1,4,8,11-tetraazacyclotetradecanenickel(II)] monohydrate, (VII), monoclinic C2/c, Z' = 0.5]. In 1,2,4,5-benzenecarboxylate tris[1,4,8,11-tetraazacyclotetradecanenickel(II)] diperchlorate hydrate (VIII), [Ni(cyclam)]3*[1,2,4,5-benzenetetracarboxylate(4-)]*[ClO4]2*[H2O]3, there are two distinct Ni sites: [Ni(cyclam)]2+ and centrosymmetric [C10H2O8]4- units form a two-dimensional coordination polymer, whose sheets are linked by centrosymmetric [Ni(cyclam)(H2O)2]2+ cations.
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http://dx.doi.org/10.1107/s010876810101850x | DOI Listing |
J Environ Manage
January 2025
Universidad Autónoma de Nuevo León, Facultad de Agronomía, Laboratorio de Ciencias Naturales, General Escobedo, 66050, Nuevo Leon, Mexico. Electronic address:
The chemical co-precipitation method was used to synthesize a variety of pure BiO and substituted BiCoCdO NPs (x = 0.0-0.8) and doping influences were evaluated based on the optical, photocatalytic, morphological, and structural characteristics.
View Article and Find Full Text PDFHeliyon
April 2024
Department of Chemistry, Annamalai University, Annamalainagar, 608 002, India.
The hydrated sodium salt of 1,2,3,4-tetrahydroquinolinedithiocarbamate ( has been successfully synthesized and characterized using IR, NMR, and X-ray single crystal analysis. The υC-S and thioureide υC-N bands appeared at 1484 cm and 968 cm, respectively, in Na(H2O)(thqdtc) • HO. The notable NCS carbon signal emerged at 212 ppm, credited to unique nitrogen and sulfur-induced deshielding effects.
View Article and Find Full Text PDFJ Chem Phys
February 2024
School of Science, Nanjing University of Posts and Telecommunications, Nanjing 210023, China.
To control the growth of layered two-dimensional structures, such as transition metal dichalcogenide materials or heterostructures, understanding the growth mechanism is crucial. Here, we report the synthesis of ultra-thin MoO2 nanoplatelets through the sublimation of MoO3. Rhombus MoO2 nanoplatelets with the P21/c space group were characterized using various microscopic and spectroscopic techniques.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2023
Department of Chemistry, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea.
Construction of three-dimensional (3D) frameworks maintaining intrinsic photophysical properties of monomeric building blocks is difficult and challenging due to the existence of various molecular interactions, such as metal-organic and π-π interactions. A 3D hydrogen-bonded organic framework () with permanent porosity was constructed using a porphyrin having six carboxylic acid groups (). Brunauer-Emmett-Teller surface area measurement indicated that has a porous structure with a surface area of 392 m/g.
View Article and Find Full Text PDFJ Inorg Biochem
January 2024
Guangxi University of Chinese Medicine, Nanning 530001, China. Electronic address:
Six half-sandwich Ru(II) complexes (Ru1-Ru6), integrated with 5-phenyl-2-(pyridin-2-yl)-2,4-dihydro-3H-pyrazol-3-one (PDPO1-PDPO6) ligands, were synthesized and spectroscopically characterized. The structure of Ru3 that crystallized as a monoclinic crystal with P21/c space group was further confirmed by X-ray single crystal diffraction. Prototropic tautomerism within the complexes transformed OH-form ligands to NH-form, forming a hydrogen bond (Cl---H-N).
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