1995
DOI: 10.1021/ic00129a010
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Synthesis, 77Se and 119Sn NMR Study, and X-ray Crystal Structure of the Sn4Se104- Anion and Raman Spectra of SnSe44- and Sn4Se104-

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Cited by 50 publications
(58 citation statements)
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“…Simulation of mirror charges31 allowed the theoretical treatment of the highly charged molecules. The calculated SnSe distances in the Co/Sn/Se cluster anions tended to be larger than the experimentally observed ones; a comparable situation was found for the results of calculations on the [Sn 4 Se 10 ] 4− ion27 (SnSe t : +4 to +5 pm, Sn(μ 2 ‐Se): +7 to +10 pm with respect to the crystallographically determined values). In contrast, the computed CoSe bond lengths in the ternary anions were all somewhat shorter than the experimental ones, which likewise was in accordance with the results of calculations on the adamantane‐type anion [{Co(SPh)} 4 (μ 2 ‐SPh) 6 ] 2− 32 (CoS: −3 to −4 pm with respect to the crystallographically determined values).…”
Section: Methodssupporting
confidence: 78%
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“…Simulation of mirror charges31 allowed the theoretical treatment of the highly charged molecules. The calculated SnSe distances in the Co/Sn/Se cluster anions tended to be larger than the experimentally observed ones; a comparable situation was found for the results of calculations on the [Sn 4 Se 10 ] 4− ion27 (SnSe t : +4 to +5 pm, Sn(μ 2 ‐Se): +7 to +10 pm with respect to the crystallographically determined values). In contrast, the computed CoSe bond lengths in the ternary anions were all somewhat shorter than the experimental ones, which likewise was in accordance with the results of calculations on the adamantane‐type anion [{Co(SPh)} 4 (μ 2 ‐SPh) 6 ] 2− 32 (CoS: −3 to −4 pm with respect to the crystallographically determined values).…”
Section: Methodssupporting
confidence: 78%
“…The SnSe bond lengths in 1 (SnSe t 247.8(2), 249.0(1) pm, Sn(μ 2 ‐Se) 250.9(1)–252.8(1) pm) correspond with those of the adamantane‐type selenostannate( IV ) anion in [2,2,2‐crypt‐K] 4 [Sn 4 Se 10 ]27 (2,2,2‐crypt=4,7,13,16,21,24‐hexaoxa‐1,10‐diazabicyclo[8.8.8]hexacosane). The Co(μ 2 ‐Se) and Co(μ 4 ‐Se) distances are very similar (Co(μ 2 ‐Se) 242.5(2)–244.8(1) pm; Co(μ 4 ‐Se) 243.6(1), 245.0(2) pm).…”
Section: Methodsmentioning
confidence: 99%
“…Another characteristic mode for the SnSe44 unit is peaks appeared at 212 and 205 cm −1 for z = 0.4 and z = 1, respectively. These peaks can be assigned to symmetric Sn–Se stretching . Therefore, the Raman spectra verify successful dual substitutions of Sn and Se on P and S sites, respectively.…”
Section: Resultsmentioning
confidence: 61%
“…The broad asymmetric peak in the range of 325–385 cm −1 observed in SnSe 2 ‐doped samples was associated with the A 1 mode of SnS44; this peak may be distinguished at 346 cm −1 in the pristine sample. The appearance of a peak at 251 cm −1 for samples where z ≠ 0 can be associated with two modes: asymmetric stretching of tetrahedral SnSe44 and symmetric bending of PS4zSez3 . The PS43 peak at 275 cm −1 coexisted with the peak of the SnSe44 unit for z = 0.4 and nearly completely disappeared when Sn fully substituted Ge.…”
Section: Resultsmentioning
confidence: 95%
“…Die im komplexen Anion von 1 bestimmten Sn‐Se‐Bindungslängen (Sn‐Se t 247.8(2)–249.0(1) pm, Sn‐(μ 2 ‐Se) 250.9(1)–252.8(1) pm) entsprechen denen des adamantanartigen Selenotetrastannat( IV )‐Anions in [2,2,2‐crypt‐K] 4 [Sn 4 Se 10 ]27 (2,2,2‐crypt=4,7,13,16,21,24‐Hexaoxa‐1,10‐diazabicyclo[8.8.8]hexacosan). Zwischen den Co‐(μ 2 ‐Se)‐ und Co‐(μ 4 ‐Se)‐Bindungslängen bestehen nahezu keine Unterschiede (Co‐(μ 2 ‐Se) 242.5(2)–244.8(1) pm, Co‐(μ 4 ‐Se) 243.6(1), 245.0(2) pm).…”
Section: Methodsunclassified