<p>The basic building blocks in molecular electronics often correspond to conjugated molecules. A compound class consisting of rigid rod-like staffane molecules with the heavier Group 14 elements Si, Ge, Sn and Pb at their bridgehead positions has now been investigated. Herein these oligomers are called heavy-core or Si-, Ge-, Sn- or Pb-core staffanes. These compounds benefit from interaction through their bicyclo[1.1.1]pentane monomer units. Quantum chemical calculations were performed to probe their geometries, stabilities and electronic properties associated with conjugation.</p><p>The stabilities of the bicyclo[<i>n.n.n</i>]alkane and [<i>n.n.n</i>]propellanes (1 ≤ <i>n</i> ≤ 3) with C, Si, Ge and Sn at the bridgehead positions were studied by calculation of homodesmotic ring strain energies. The bicyclic compounds with <i>n</i> = 1 and Si, Ge or Sn at bridgehead positions have lower strain than the all-carbon compound.</p><p>A gradually higher polarizability exaltation is found as the bridgehead element is changed from C to Si, Ge, Sn or Pb. The ratio between longitudinal and average polarizability also increases gradually as Group 14 is descended, consistent with enhanced conjugation in the heavier oligomers.</p><p>The localization of polarons in C-, Si- and Sn-core staffane radical cations was calculated along with internal reorganization energies. The polaron is less localized in Si- and Sn-core than in C-core staffane radical cation. The reorganization energies are also lower for the heavier staffanes, facilitating hole mobility when compared to the C-core staffanes.</p><p>The effect of the bicyclic structure on the low valence excitations in the UV-spectra of compounds with two connected disilyl segments was also investigated. MS-CASPT2 calculations of 1,4-disilyl- and 1,4-bis(trimethylsilyl)-1,4-disilabicyclo[2.2.1]heptanes and 1,4-disilyl- and 1,4-bis(trimethylsilyl)-1,4-disilabicyclo[2.1.1]hexanes revealed that although the bicyclic cage separates the two disilyl chromophores, there is a strong red-shift of the lowest valence excitations when compared to an isolated disilane.</p>
| Identifer | oai:union.ndltd.org:UPSALLA/oai:DiVA.org:uu-7492 |
| Date | January 2007 |
| Creators | Sandström, Niclas |
| Publisher | Uppsala University, Department of Biochemistry and Organic Chemistry, Uppsala : Acta Universitatis Upsaliensis |
| Source Sets | DiVA Archive at Upsalla University |
| Language | English |
| Detected Language | English |
| Type | Doctoral thesis, comprehensive summary, text |
| Relation | Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 1651-6214 ; 271 |
Page generated in 0.0062 seconds