2002
DOI: 10.1002/1521-3749(200208)628:8<1868::aid-zaac1868>3.0.co;2-r
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Preparation and Crystal Structure of Copper(I) Carbonyl Hydrogensulfate, obtained by Carbonylation in Sulphuric AcidDedicated to Professor Joachim Strähle on the Occasion of his 65th Birthday

Abstract: The hydrogensulfato-carbonyl derivative [Cu(CO)-(SO 4 H)] n , as obtained from the Cu 2 O/ H 2 SO 4 /CO system and recrystallized from H 2 SO 4 /(CH 3 O) 2 SO 2 has been shown to possess a crystal structure organised in infinite chains built up by corner sharing of {CuO 3 (CO)} and {S(OH)O 3 } tetrahedra. The chains are connected by hydrogen bonds in layers, with CO groups leaning

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Cited by 6 publications
(5 citation statements)
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“…Bond lengths for Cu−C are 1.811(5), 1.819(3), and 1.828(4) Å and for C⋮O are 1.108(5), 1.120(4), and 1.126(5) Å for 3a − c , respectively. These values are well within the range of known copper carbonyl species (Cu−C−O range 169.2−180.0°, Cu−C range 1.660−1.968 Å, C⋮O range 1.043−1.198 Å). Dihedral angles (C−Cu···Cu−C) between carbonyls on either side of a DABCO ligand are approximately 89.6° and those on either side of a Pip ligand are 68.6°, while those across a Cu 2 Cl 2 dimer are exactly 180°. Since all non-hydrogen atoms in 3c except chlorines and the ring carbons lie on the ac plane, all C−Cu···Cu−C dihedral angles for both carbonyls and DMP methyls are 180°.…”
Section: Resultssupporting
confidence: 64%
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“…Bond lengths for Cu−C are 1.811(5), 1.819(3), and 1.828(4) Å and for C⋮O are 1.108(5), 1.120(4), and 1.126(5) Å for 3a − c , respectively. These values are well within the range of known copper carbonyl species (Cu−C−O range 169.2−180.0°, Cu−C range 1.660−1.968 Å, C⋮O range 1.043−1.198 Å). Dihedral angles (C−Cu···Cu−C) between carbonyls on either side of a DABCO ligand are approximately 89.6° and those on either side of a Pip ligand are 68.6°, while those across a Cu 2 Cl 2 dimer are exactly 180°. Since all non-hydrogen atoms in 3c except chlorines and the ring carbons lie on the ac plane, all C−Cu···Cu−C dihedral angles for both carbonyls and DMP methyls are 180°.…”
Section: Resultssupporting
confidence: 64%
“…As part of our ongoing studies of Cu(I) coordination polymers, we are investigating the reactions of copper(I) halides with bridging ligands in the presence of carbon monoxide. Numerous Cu(I)−carbonyl complexes are known; however, only a few polymeric crystal structures containing Cu−CO have been reported. These include that of CuCl(CO) itself, which forms a hexagonal honeycomb layer structure via triply bridging chloride .…”
Section: Introductionmentioning
confidence: 99%
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“…Uncharacteristically for the soft copper(I) ion, the CuCO unit is often found coordinated to the oxygen donor anions: alkoxide, carboxylate, sulfonate, and phosphonate . These complexes, which are usually formed under 1 atm of CO, form oligomers and polymers, such as III – V . , The cubane geometry reflected in III is very common for Cu(I), most commonly being encountered with μ 3 -halide corners.…”
Section: Copper(i) Carbonylsmentioning
confidence: 99%
“…On the other hand, only a limited number of copper(I) coordination polymers containing a Cu−CO unit have been structurally characterized. All reported copper(I) carbonyl polymers with polydentate ligands, either with N-containing bridging ligands such as diazabicyclo[2.2.2]octane, piperazine, N , N ‘-dimethypiperazine, and 1,2-di-2-pyridylethylene 11c,f or with polyoxygen anions such as ethyl sulfonate, hydrogen sulfate, and trichloroacetate, 11a,d,e exhibit chain structures. Only [CuCl(CO)] n , a compound without a supporting organic ligand, shows a hexagonal honeycomb layer structure,11b and it represents the only reported two-dimensional copper(I) carbonyl polymer.…”
Section: Introductionmentioning
confidence: 99%