168 research outputs found
Synthesis of Two New Group 13 Benzoato-Chloro Complexes: A Structural Study of Gallium and Indium Chelating Carboxylates
Two new heteroleptic chelated-benzoato gallium (III) and indium (III) complexes have been prepared and structurally characterized. The molecular structures of [GaCl2(4-Mepy)2(O2CPh)]4-Mepy (1) and [InCl(4-Mepy)2(O2CPh)2]4-Mepy (2) have been determined by single-crystal x-ray diffraction. The gallium compound (1) is a distorted octahedron with cis-chloride ligands co-planar with the chelating benzoate and the 4-methylpyridines trans to each other. This is the first example of a Ga(III) structure with a chelating benzoate. The indium compound (2) is a distorted pentagonal bipyramid with two chelating benzoates, one 4-methylpyridine in the plane and a chloride trans to the other 4-methylpyridine. The indium bis-benzoate is an unusual example of a seven-coordinate structure with classical ligands. Both complexes, which due to the chelates, could also be described as pseudo-trigonal bipyramidal, include a three-bladed motif with three roughly parallel aromatic rings that along with a solvent of crystallization and electron-withdrawing chloride ligand(s) stabilize the solid-state structures
Bifunctional Electrolytes For Lithium-Ion Batteries
https://commons.case.edu/research-showcase/1006/thumbnail.jp
From rock-stable to reactive phosphorus
A low-temperature route converts phosphate into an anion useful in chemical synthesis</jats:p
Organoiodine(III) Reagents as Active Participants and Ligands in Transition Metal-Catalyzed Reactions: Iodosylarenes and (Imino)iodoarenes
‘Phospha-Wittig’ reactions using isolable phosphoranylidenephosphines ArPPR3 (Ar = 2,6-Mes2C6H3 or 2,4,6-But3C6H2)
‘Phospha-variations’ on the themes of Staudinger and Wittig: phosphorus analogs of Wittig reagents
Phosphorus as a carbon copy and as a photocopy: New conjugated materials featuring multiply bonded phosphorus
Phosphaalkenes (RP=CR2) and diphosphenes (RP=PR) are main group analogues of alkenes (R2C=CR2). Molecules featuring such multiply bonded phosphorus functionalities often display structural features and chemical reactivities that mimic their purely organic counterparts, lending credence to the claim that these compounds are “carbon copies”. We have been expanding this analogy to include oligomers and polymers with extended conjugation that directly involve P=C and P=P units. Many of these materials, however, display little or no photoluminescence (PL). This article summarizes our efforts to understand P=C and P=P photobehavior and to produce materials having significant PL that mimic or “photocopy” the PL properties of the phosphorus-free systems. Recent materials based on benzoxaphospholes (BOPs), benzobisoxaphospholes (BBOPs), and higher analogues having significant fluorescence quantum yields are covered.</jats:p
Development of new hypervalent iodine reagents with improved properties and reactivity by redirecting secondary bonds at iodine center
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