Virginia Polytechnic Institute and State University
Bond length and bonded radii variations in sulfide molecules and crystals containing main group elements
Abstract
dc:description.abstractMolecular orbital calculations on 18 hydrosulfide molecules containing selected main group X-cations yield minimum energy bond lengths, R<sub>t</sub>(XS), that reproduce those observed in chemically similar sulfide crystals. A least-squares analysis shows that R<sub>t</sub>(XS) can be estimated by the equation R = l.83(s/r)<sup>-0.21</sup>, where s is the Pauling bond strength and r is the row number of the X-cation in the periodic table, with 98% of the variation of R<sub>t</sub>(XS) being explained in terms of a linear dependence on R. In addition, R serves to rank observed XS bond lengths in sulfide crystals for main group X-cations for rows 1 through 5 of the periodic table to within 0.12Å on average, with R accounting for 96% of the variation in the observed bond lengths. Bonded radii obtained from electron density maps calculated for the molecules show that the radii of both the X-cations and S atom increase with R<sub>t</sub>(XS). A similar trend has been found to hold for the bonded radii and the R<sub>t</sub>(XO) bond lengths calculated for hydroxyacid molecules (Finger and Gibbs 1985). The radius of S is smaller (1.16Å) when bonded to highly electronegative atoms like 4-coordinate As and larger (1.67Å) when bonded to a considerably less electronegative atoms like 4-coordinate Li but is smaller than Shannon's (1.70Å) crystal radius and Pauling's ionic crystal radius (1.84Å).
Degree
thesis:*- Name thesis:degree_name
- M.S.
- Level thesis:degree_level
- masters
- Discipline thesis:degree_discipline
- Geological Sciences
- Department dc:contributor.department
- Geological Sciences
- Grantor dc:publisher
- Virginia Polytechnic Institute and State University
- Year dc:date.issued
- 1987
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Bartelmehs, Kurt Lane
Rights
dc:rights- Statement dc:rights
-
- In Copyright
- Licence dc:rights.uri
- Language dc:language.iso
- en_US
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- http://hdl.handle.net/10919/91160
- OAI identifier oai:identifier
- oai:vtechworks.lib.vt.edu:10919/91160