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The reference covalent bond distances are as follows: CH 3BH2 (Cs, 1.554; SiH3BH 2 (Cs, 2.017; GeH3BH2 (Cs, 2.066; SnH3BH2 (C s, 2.258; PbH3-BH2 (Cs, 2.304; B2H4 (D2d, 1.629; B 2H2 D8h, 1.507 Å. CH 3BH2, SiH3-BH2, GeH 3BH2, B2H4, and B2H 2 geometries are optimized at B3LYP/6-311++G** level, and SnH3BH2 and PbH3BH2 geometries were optimized at B3LYP/def2-TZVPP level. For additional covalent bond distance reference, see Suresh, C. H, Koga, N. J. Phys. Chem. A 2001, 105, 5940
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When compared to a hypothetical model of D6h SnB 62- with short Sn-B distance (constrained to 1.8 Å, a highly unfavorable anti-bonding B-B interaction (b1u MO; see Figure 1-SI) are now reduced due to the long B-B distance in triplet D6h SnB62, Meanwhile, bonding e1g π MOs become less stable due to the increased B-B distance, resulting in the inversion of occupied (e 1g) and the unoccupied b1u, so that b1u MO is fully occupied, leaving degenerate e1g π MOs singly occupied. Hence, SnB 62- and, similarly, PbB62- are triplet ground states
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2- are triplet ground states.
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88
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In SnB7, PbB7, and PbB 8, the anti-bonding a1 interaction is diminished as the central atom moves away from the Bn rings, whereas radial bonding e1 MO interactions become less stable, resulting in the inversion of a1 and e2 MOs see Figure 2-SI, Hence, a1 MO is fully occupied and e2 MOs are singly occupied in SnB7, PbB7, and PbB8
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8.
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