Data collection can be performed at the temperature range 80 - 320 K. Furthermore, a great deal of consulting services are offered for the local community and other teaching and research institutes in Jordan. BRUKER APEX II Diffractometer can be used to obtain powder patterns of samples sealed in 0.3 -1 mm capillaries. Fill in the following parameters and then click the Convert button to convert the frames Images from: select the image files to convert Output format: select the. This lab serves the teaching at undergraduate and graduate levels and research at the Geology Department and also supports research of other departments at the University of Jordan.

Semi-quantitative determination of amounts of different phases in multi-phase mixtures (i.e rocks and industrial mixtures) using suitable standards and peak-ratio calculations.

Recognition of amorphous materials in partially crystalline mixtures.

Identification and structural analysis of clay minerals, soils and industrial tissues and other micro- and cryptocrystalline materials.

minerals, chemical compounds or other engineered synthetic substances

Identification of single and multiple phase materials i.e.

The mixture was heated to 90Р В Р вЂ Р вЂ™Р’ВР В Р вЂ° and then 2.

Terephthalaldehyde (1.07 g, 8.00 mmol) and acetic acid (30 mL) were added to a flask with three necks and then ammonium acetate (0.31 g, 3.99 mmol) was added. ESI high (HRMS) were acquired on a Bruker Apex IV FTMS mass spectrometer. HRMS was performed with a Bruker Apex IV FTMS purchased from Brooke Byers Spin Co., LTD, Switzerland. Symmetry codes: (i) Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ x, y, Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ z+1/2 (ii) Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ x+1/2, Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ y+1/2, Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ z+1 (iii) Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ x, Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ y, Р В Р вЂ Р Р†РІР‚С™Р’В¬Р Р†Р вЂљРІвЂћСћ z+1.Steels, non-ferrous metals, machinery, shipbuilding, welding, automobiles, ceramics, cement, glass, catalysts, electrical parts, electronic materials, magnetic materials, superconductive materials, fibers, paper, pulp, food products, chemicals, agricultural chemicals, dies, pigments, paints, pharmaceuticals, dental materials, biological matter, petroleum, coal, power generation, natural gas, mining ore, soil, rocks, clay, minerals, construction, civil engineering, environment, and industrial waste. 1H NMR was recorded on the 400 MHz (Bruker ARX400) and 13C NMR spectra were recorded on the Bruker 125 MHz spectrometer at room temperature with CDCl3 as the solvent and tetramethylsilane (TMS) the internal standard. High resolu-tion mass spectrometry (HR-MS) was performed on an APEX IV 7T FTICR instrument by Bruker Daltonic. O hydrogen bonds (Table 2).Р В РІР‚СњР В РІР‚РЋractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Р В РІР‚СљР Р†Р вЂљР’В¦ 2) top spectra were recorded on a Bruker FT-IR Alpha-spectrometer with ATR sampling module.The crystal structure is stabilized by intramolecular O-H The propyl group becomes an ornament in the coordination network. The chains are connected through the coordination of the carboxylate O3 atoms to the Na ions, forming a three-dimensional structure (Fig. Two O1 atoms of the H 2pimdc ligand bridge two Na atoms, forming a parallelogram and two O5 atoms of the water molecules form another parallelogram with two Na atoms, leading to a chain along. The coordination of Na ion is achieved by two water molecules, one N atom and three O atoms from three H 2pimdc ligands (Fig. In the title compound, the 2-propyl-4-carboxy-1 H-imidazole-5-carboxylate (H 2pimdc) ligand is bonded to Na ions in a Р В РІР‚в„ўР вЂ™Р’Вµ 3-mode. The distinct binding modes of the ligands as well as the coordination preferences of the metal ion are discussed. Here we present the synthesis and structure of the title complex derived from 2-propyl-1 H-imidazole-4,5-dicarboxylic acid. Imidazole-4,5-dicarboxylic acid and derivatives have been studied in terms of their physical properties as well as for their diverse biological activities (Bogdanova et al., 1992 Borodkin et al., 1984 Reichardt et al., 1992), including the use of imidazole-4,5-dicarboxylic acid amides in the development of human immunodeficiency virus (HIV-1) protease inhibitors (Baures, 1999). The N atoms of imidazole can coordinate to metal ions in monodentate or bidentate mode (Su et al., 2001). 1 H-Imidazole and its derivatives are a kind of excellent supramolecular synthons.

Bruker apex iv