Structure topology and hydrogen bonding in marthozite, Cu2+[(UO2)3(SeO3)2O2](H2O)8, a comparison with guilleminite, Ba[(UO2)3(SeO3)2O2](H2O)3

被引:49
|
作者
Cooper, MA [1 ]
Hawthorne, FC [1 ]
机构
[1] Univ Manitoba, Dept Geol Sci, Winnipeg, MB R3T 2N2, Canada
来源
CANADIAN MINERALOGIST | 2001年 / 39卷
关键词
marthozite; crystal structure; chemical formula; hydrogen bonding; uranium mineral; guilleminite;
D O I
10.2113/gscanmin.39.3.797
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
The crystal structure of marthozite, Cu2+ [(UO2)(3) (SeO3)(2) O-2] (H2O)(8), a 6.9879(4), b 16.4537(10), c 17.2229(10) Angstrom, V 1980.2(3) Angstrom (3), Pbn2(1), Z = 4, D-calc = 4.37 g/cm(3), has been solved by direct methods and refined to an R index of 5.7% for 4364 observed (\F-o\ > 4 sigmaF) reflections collected with a four-circle diffractometer fitted with MoK alpha X-radiation and a CCD detector. There are three unique U sites, each occupied by U6+ with two short U-O-uranyl bonds (1.76-1.82 Angstrom) and coordination numbers of [8], [7] and [7], respectively. There are two unique Se sites, each occupied by Se4+ and coordinated by three O atoms (Se-O approximate to 1.70 A), forming a triangular pyramid with Se at the apex, indicative of stereoactive lone-pair behavior in Se4+. There is one Cu site, occupied by Cu2+ in octahedral coordination by four (H2O) groups (Cu-H2O = 2.0 Angstrom) and two O atoms (Cu-O = 2.4 Angstrom). The structural unit is a sheet of composition [(UO2)(3) (SeO3)(2) O-2], comprised of chains of edge-sharing (U phi (n)) polyhedra extending along [100] that are cross-linked in the [001] direction by (SeO3) groups; this sheet is topologically identical to the structural unit in guilleminite, Ba [(UO2)(3) (SeO3)(2) O-2] (H2O)(3). Adjacent sheets are linked through interstitial Cu2+ cations via Cu2+-O-apical bonds and via H bonds that involve both (H2O) groups bonded to Cu2+ and interstitial (H2O) groups not bonded to any cation. The principal differences between marthozite and guilleminite involve the interlayer species. In guilleminite, the Ba atom is centrally positioned with respect to the chain of(UOn) polyhedra, whereas in marthozite, the Cu2+ atom is located off the pseudo-mirror plane of the chain of (UOn) polyhedra. This differential positioning of the interstitial cations results in an intersheet separation in marthozite that is nearly 1 Angstrom greater than that in guilleminite, despite the fact that Ba (in guilleminite) is much larger than Cu2+ (in marthozite). The H-bond arrangement in marthozite is very different from that in guilleminite. In marthozite, there are eight unique interlayer (H2O) groups; four of these (H2O) groups bond directly to Cu2+ and four are held in the structure solely by H bonds. In guilleminite, there are two unique interlayer (H2O) groups, both of which bond to the interlayer Ba atoms.
引用
收藏
页码:797 / 807
页数:11
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