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The crystal structure of the title compound, hexaaquanickel(II) dichloride–1,4,7,10,13,16-hexaoxacyclooctadecane–water (1/2/2), [Ni(H2O)6]Cl2·2C12H24O6·2H2O, is reported. The asymmetric unit contains half of the Ni(OH2)6moiety with a formula of C12H32ClNi0.50O10at 105 K and triclinic (P1) symmetry. The [Ni(OH2)6]2+cation has close to ideal octahedral geometry with O—Ni—O bond angles that are within 3° of idealized values. The supramolecular structure includes hydrogen bonding between the water ligands, 18-crown-6 molecules, Cl−anions, and co-crystallized water solvent. Two crown ether molecules flank the [Ni(OH2)6]2+molecule at the axial positions in a sandwich-like structure. The relatively symmetric hydrogen-bonding network is enabled by small Cl−counter-ions and likely influences the more idealized octahedral geometry of [Ni(OH2)6]2+.
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Theoretical assessments of Pd–PdO phase transformation and its impacts on H 2 O 2 synthesis and decomposition pathways
This work highlights how Pd–O arrangements and particle sizes impact primary H2O2selectivities and yields in its direct synthesis.
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- Award ID(s):
- 1921484
- PAR ID:
- 10476256
- Publisher / Repository:
- Royal Society of Chemistry
- Date Published:
- Journal Name:
- Catalysis Science & Technology
- Volume:
- 13
- Issue:
- 13
- ISSN:
- 2044-4753
- Page Range / eLocation ID:
- 3828 to 3848
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/D3CY00404J
