Time-resolved energy dispersive X-ray diffraction (EDXRD) data have been measured in situ from cast blocks of gypsum, CaSO(4) x 2 H(2)O, in the presence of reactive phosphate solutions under hydrothermal conditions (100 < or = T < or = 180 degrees C) in order to understand the formation of hydroxyapatite monoliths, for applications such as in artificial bone or dental materials. Measurement of data in short (60 s) intervals has thus permitted information about the kinetics and mechanism of transformation of gypsum to hydroxyapatite to be obtained in a non-invasive way, avoiding the irreversible conversion of hydrous intermediate phases that would occur on quenching. At the lower temperatures used gypsum first converts to an amorphous intermediate phase during reaction, but as the temperature is raised to 130 degrees C and above, hydrothermal dehydration to the subhydrate CaSO(4) x 1/2 H(2)O always occurs before hydroxyapatite crystallises. The final crystal size of the hydroxyapatite is estimated from the peak broadening of the EDXRD data and this reveals an increase in crystal dimension with increasing reaction temperature. Comparing measurements from the surface and from the core of the blocks shows that an additional phosphate phase, CaHPO(4), is observed in the core at two temperatures and also that the crystal growth of hydroxyapatite does not penetrate the core of the block on the time scales we have investigated (up to 6 hours). The observations have important implications in the fabrication of hydroxyapatite monoliths from cast gypsum for applications, since the conversion via several intermediate phases may compromise the integrity and mechanical properties of the monoliths.
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http://dx.doi.org/10.1039/b910485m | DOI Listing |
Inorg Chem
January 2025
Institute for Inorganic Chemistry and Center for Sustainable Systems Design (CSSD), Paderborn University, Paderborn 33098, Germany.
A series of Co complexes [Co(ImP)][PF], with HImP = 1,1'-(1,3-phenylene)bis(3-methyl-1-imidazole-2-ylidene)) and R = Me, Et, Pr, Bu, is presented in this work. The influence of the strong donor ligand on the ground and excited-state photophysical properties was investigated in the context of different alkyl substituents at the imidazole nitrogen. X-ray diffraction revealed no significant alterations of the structures and all differences in the series emerge from the electronic structures.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry, University of Southern California, Los Angeles, California 90089, United States.
The photophysical properties of six new luminescent tetrahedral Zn(II) complexes are presented that survey two electronic donor moieties (phenolate and carbazolate) and three electronic acceptors (pyridine, pyrimidine, and pyrazine). A unique ligand based on an -terphenyl motif forms an eight-membered chelate, which enhances through-space charge-transfer (CT) interactions by limiting through-bond conjugation between the donor and acceptor. A single isomeric product was obtained in yields up to 90%.
View Article and Find Full Text PDFLangmuir
January 2025
College of Chemistry and Molecular Engineering, Nanjing Tech University, Nanjing 211816, P.R. China.
Morphology regulation and element doping are effective means to improving the photocatalytic performance of graphite-phase carbon nitride (g-CN). In this article, using melamine and zinc chloride as raw materials, a novel kind of Zn/Cl-doped hollow microtubular g-CN (Zn-HT-CN) by a hydrothermal method was developed. The structure and morphology of Zn-HT-CN and reference samples were characterized by X-ray diffraction patterns (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), etc.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
New Chemistry Unit, International Centre for Materials Science and School of Advanced Materials, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore, Jakkur P.O. 560064, India.
Seeking new and efficient thermoelectric materials requires a detailed comprehension of chemical bonding and structure in solids at microscopic levels, which dictates their intriguing physical and chemical properties. Herein, we investigate the influence of local structural distortion on the thermoelectric properties of TlCuS, a layered metal sulfide featuring edge-shared Cu-S tetrahedra within CuS layers. While powder X-ray diffraction suggests average crystallographic symmetry with no distortion in CuS tetrahedra, the synchrotron X-ray pair distribution function experiment exposes concealed local symmetry breaking, with dynamic off-centering distortions of the CuS tetrahedra.
View Article and Find Full Text PDFOrg Biomol Chem
January 2025
Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China.
(±)-Melichuniiones A and B (1 and 2), two novel enantiomeric pairs of lignan-phloroglucinol hybrids with an unprecedented beadlike core were isolated from the leaves of , together with new analogues 3-6. Compounds 1 and 2 possess a unique dispiro [furan-2,5'-cyclopenta[]furan-2',3''-furan] 5/5/5/5 tetracyclic skeleton. Their structures were established by extensive spectroscopic analyses, single crystal X-ray diffraction, and electronic circular dichroism (ECD) calculations.
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