144094-96-2Relevant academic research and scientific papers
Monitoring the formation of carbide crystal phases during the thermal decomposition of 3d transition metal dicarboxylate complexes
Huba, Zachary J.,Carpenter, Everett E.
, p. 12236 - 12242 (2014)
Single molecule precursors can help to simplify the synthesis of complex alloys by minimizing the amount of necessary starting reagents. However, single molecule precursors are time consuming to prepare with very few being commercially available. In this study, a simple precipitation method is used to prepare Fe, Co, and Ni fumarate and succinate complexes. These complexes were then thermally decomposed in an inert atmosphere to test their efficiency as single molecule precursors for the formation of metal carbide phases. Elevated temperature X-ray diffraction was used to identify the crystal phases produced upon decomposition of the metal dicarboxylate complexes. Thermogravimetric analysis coupled with an infrared detector was used to identify the developed gaseous decomposition products. All complexes tested showed a reduction from the starting M2+ oxidation state to the M0 oxidation state, upon decomposition. Also, each complex tested showed CO2 and H 2O as gaseous decomposition products. Nickel succinate, iron succinate, and iron fumarate complexes were found to form carbide phases upon decomposition. This proves that transition metal dicarboxylate salts can be employed as efficient single molecule precursors for the formation of metal carbide crystal phases.
Catena-poly[[tetraaquairon(II)]-μ-succinato-K2O:O′]
Xu, Tu-Gen,Xu, Duan-Jun,Wu, Jing-Yun,Chiang, Michael Y.
, p. m615-m616 (2007/10/03)
The title complex, {[Fe(C4H4O4)(H2O)4]} n, is an infinite polymeric compound bridged by the succinate dianion. Two carboxylate groups coordinate in a monodentate manner to the FeII atom, in a trans fashion, with an O-Fe-O bond angle of 175.72(6)° and Fe-O distances of 2.0886 (14) and 2.1008 (15) A. One of the uncoordinated carboxylate O atom forms an intramolecular hydrogen bond with a coordinated water molecule. Extensive hydrogen bonding between parallel polymeric complex chains results in a three-dimensional supramolecular structure.
