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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Chikkali, Samir H.
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article
Boron templated catechol phosphines as bidentate ligands in silver complexes
Abstract
Reaction of 3-[(diphenylphosphinyl)methyl] benzene-1,2-diol (1) and 4-[(diphenylphosphinyl)methyl]benzene-1,2-diol (2) with AgOTf or B(OH)(3) produced the bis-phosphine complexes 4, 5, or the borates 6, 7, respectively. All products were characterised by analytical and spectroscopic data and single-crystal X-ray diffraction studies. The anionic assembly 6 was shown to act as a template-based chelate ligand toward Ag+ by forming a neutral complex 8 of composition [(6)Ag] with AgOTE Spectroscopic and single-crystal X-ray diffraction studies revealed the presence of a kinetically very stable and conformationally rigid chelate that is best described as a bis-phosphine silver complex with a distinctly non-linear P-Ag-P array and two further secondary Ag-O interactions. Reaction of 7 with AgOTf proceeded in a 2 : 2 molar ratio to give a dimeric product 9 which was, on the basis of spectroscopic data, formulated as a macrocycle of composition [(7)(2)Ag-2]. The different molecular sizes of 8 and 9 was underlined by PGSE NMR measurements which gave further evidence for the formation of solvent adducts between the chelate complex 8 and DMF. Analysis of the H-1,Ag-109 HMQC NMR spectra of 8 provided evidence for a dependence of the (3)JAg center dot H coupling on torsional angles which resembles a Karplus-type relationship.