Creating Optical Activity: Total Spontaneous Resolution and Viedma Ripening
Date
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Abstract
The creation of optical activity has been considered as something impossible even though reports of such creation via total spontaneous resolution since the 1940´s have been published. More recently Viedma ripening have been developed that also produce enantiopure bulk product. Both methods are examples of absolute asymmetric synthesis i.e. the synthesis of optically active product from non-optically active starting materials, catalysts or auxiliaries. In this work twenty-four new compounds have been synthesized, isolated and characterized with X-ray diffraction. Out of these have eleven been found to crystallize as conglomerates as chiral enantiopure crystals which are optically active. The discovered conglomerates have been analyzed with solid state techniques as circular dichroism (CD) and vibrational circular dichroism(VCD). For the moderately labile [Ru(PS)2Cl2], [Ru(dmso)2(NS)Cl2 and [Ru(dmso)2(SS)Cl2] have the chirality been fixated by oxidizing the ligand in solution to the corresponding sulfoxide. For the highly labile Co(bpy)32 the chirality has been fixated by oxidizing the metal from cobalt(II), solvent free in the solid state, to the inert cobalt (III) with bromine vapor or solid iodine. The optical activity of the inert complexes has been analyzed with solution techniques such as CD, HPLC and ORD. The optical activity of the complexes [Mo(CO)4PS] and [W(CO)4PS] have been analyzed with solid state VCD with less than tenth of a milligram sample and high-quality spectra have been obtained in 20 minutes. Total spontaneous resolution has been achieved with the compounds [Ru(PS)2Cl2], [Ru(dmso)2(NS)Cl2, [Ru(dmso)2(SS)Cl2] and Ag(PS)2 in good yield and high ee. Viedma ripening has been demonstrated for the complexes Ag(PS)2, [Mo(CO)4PS], [W(CO)4PS] and [Cu(mtp)2(NO3)2]. Viedma ripening has been found to be viable for the production of large quantities of optically pure metal complex.
Description
Keywords
Citation
ISBN
Articles
II. Theonitsa Kokoli, Susanne Olsson, Per Martin Björemark, Staffan Persson and Mikael Håkansson. Toward absolute asymmetric synthesis of coordination polymers with bidentate sulfide ligands. Journal of Organometallic Chemistry, 2013 (724), 17-22. ::doi::10.1016/j.jorganchem.2012.10.035
III. Theonitsa Kokoli, Susanne Olsson, Per Martin Björemark, Jonas Sundberg, Anders Lennartsson, Christine J. McKenzie and Mikael Håkansson. Absolute asymmetric synthesis: Protected substrate oxidation. Chemistry-a European Journal, 2015 (21), 13, 5211-5219. ::doi::10.1002/chem.201406354
IV. Per Martin Björemark, Susanne Olsson, Theonitsa Kokoli, Mikael Håkansson. Absolute Asymmetric Synthesis of a Tetrahedral Silver Complex. Chemistry-a European Journal, 2015 (21), 24, 8750-8753. ::doi::10.1002/chem.201500986
V. Per Martin Björemark, Johan Jönsson and Mikael Håkansson. Absolute Asymmetric Synthesis: Viedma Ripening of Co(bpy)3(2+) and Solvent-Free Oxidation to Co(bpy)3(3+). Chemistry-a European Journal, 2015 (21), 30 10630-10633. ::doi::10.1002/chem.201500876
VI. Per Martin Björemark and Mikael Håkansson. Viedma Ripening of Group VI Metal Carbonyl Complexes. Manuscript.
VII. Per Martin Björemark, Jonas Sundberg, Vibe B. Jacobsen, Christine J. McKenzie, and Mikael Håkansson. Grinding Achiral Crystals to Enantiopurity. Manuscript