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Heterolysis of Dihydrogen by Silver Alkoxides and Fluorides.

Chemistry (Weinheim an der Bergstrasse, Germany) (2015-06-11)
Brandon K Tate, Jenna T Nguyen, John Bacsa, Joseph P Sadighi
ZUSAMMENFASSUNG

Alkoxide-bridged disilver cations react with dihydrogen to form hydride-bridged cations, releasing free alcohol. Hydrogenolysis of neutral silver fluorides affords hydride-bridged disilver cations as their bifluoride salts. These reactions proceed most efficiently when the supporting ligands are expanded N-heterocyclic carbenes (NHCs) derived from 6- and 7-membered cyclic amidinium salts. Kinetics studies show that silver fluoride hydrogenolysis is first-order in both silver and dihydrogen.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Deuteriumoxid, 99.9 atom % D
Sigma-Aldrich
Acetonitril, anhydrous, 99.8%
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Tetrahydrofuran, anhydrous, ≥99.9%, inhibitor-free
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Dichlormethan, anhydrous, ≥99.8%, contains 40-150 ppm amylene as stabilizer
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Toluol, anhydrous, 99.8%
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Tetrahydrofuran, anhydrous, contains 250 ppm BHT as inhibitor, ≥99.9%
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Deuteriumoxid, 99.9 atom % D, contains 0.05 wt. % 3-(trimethylsilyl)propionic-2,2,3,3-d4 acid, sodium salt
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Lithiumaluminiumhydrid, powder, reagent grade, 95%
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Benzol, anhydrous, 99.8%
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Deuteriumoxid, 99.9 atom % D, contains 0.75 wt. % 3-(trimethylsilyl)propionic-2,2,3,3-d4 acid, sodium salt
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1,4-Dimethoxybenzol, ReagentPlus®, 99%
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Deuterium, 99.8 atom % D
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Pentan, anhydrous, ≥99%
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Lithiumaluminiumhydrid, pellets, reagent grade, 95%
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1,4-Dimethoxybenzol, 99%, FG
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Calciumhydrid, reagent grade, 95% (gas-volumetric)
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Supelco
Tetrahydrofuran, HPLC grade, ≥99.9%, inhibitor-free
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