2000
DOI: 10.1023/a:1004167901190
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Cited by 9 publications
(10 citation statements)
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“…The halogen derivatives contained halogen atoms at the positions 5, 6 [19], 2, 4 [20], and 3 [21] in the ''lower'' belt of the 7,8-dicarba-nido-undecaborate cage can be obtained by indirect methods. The bromination and iodination at the ''lower'' belt of [9-Py-7,8-C 2 B 9 H 11 ] was reported earlier by Volkov et al [15], however, the proposed position of substitution was not supported by any reasonable arguments. Moreover, these results (at least in the iodination part) were disproved later by X-ray structure determination, which revealed the substitution at the position 11 of the ''upper'' belt [16].…”
Section: Resultsmentioning
confidence: 85%
See 1 more Smart Citation
“…The halogen derivatives contained halogen atoms at the positions 5, 6 [19], 2, 4 [20], and 3 [21] in the ''lower'' belt of the 7,8-dicarba-nido-undecaborate cage can be obtained by indirect methods. The bromination and iodination at the ''lower'' belt of [9-Py-7,8-C 2 B 9 H 11 ] was reported earlier by Volkov et al [15], however, the proposed position of substitution was not supported by any reasonable arguments. Moreover, these results (at least in the iodination part) were disproved later by X-ray structure determination, which revealed the substitution at the position 11 of the ''upper'' belt [16].…”
Section: Resultsmentioning
confidence: 85%
“…An introduction of alkyl or aryl substituents at the carbon atoms of the carborane cage does not interfere with this pattern [11][12][13][14]. The halogenation of charge-compensated nido-carboranes is less studied [15], however the iodination of [9-Py-7,8-C 2 B 9 H 11 ] with elemental iodine has been reported recently to proceed at the position 11 giving [9-Py-11-I-7,8-C 2 B 9 H 10 ] [16]. Based on these data it could be expected that halogenation of [9-Me 2 S-7,8-C 2 B 9 H 11 ] will proceed in the similar way.…”
Section: Resultsmentioning
confidence: 99%
“…Later in 2000, Volkov et al further investigated the photophysical properties of a series of cluster borane derivatives, carboranes of the types B 10 H 12 [Py(X)] 2 , C 2 B 9 H 11 Py(X) and C 2 B 9 H 10 BrPy(X) and the salts of hydroborate anions [B 10 H 13 Py(X)] À , [B 10 H 10 ] 2À and [B 12 H 12 ] 2À with cations of quaternary pyridinium bases. 68 On the basis of the studies into the key photoluminescence properties of a series of forty two compounds, it was demonstrated that the luminescence features are rather inherent for boron hydrides. However, neutral boranes seldom show any detectable photoluminescence.…”
Section: Boranes and Their Derivativesmentioning
confidence: 99%
“…Previously [1] we revealed weak ferromagnetic interactions at 20 K in the complexes [MnPhen 3 ][Co(C 2 . B 9 H 11 ) 2 ] 2 and [MnPhen 3 ][C 2 B 9 H 12 ] 2 [Phen is phenanthroline, 1,10-C 12 H 8 N 2 ; C 2 B 9 H 12 is the dodecahydro-7,8-dicarba-nido-undecaborate (13) anion] containing the paramagnetic Mn(II) ion (3d 5 ), which is a new fact in the chemistry of boron hydrides. Here we report on a compound containing the 1,2;1`,2`-trans-bis-[nonahydro-closo-decaborate] (23) anion, [B 20 H 18 ] 2!…”
mentioning
confidence: 99%
“…In particular, whereas the spectrum of the [B 10 H 10 ] 2! anion consists of two signals with the intensity ratio of 1 : 4 and 2523 cm !1 , respectively, which suggests a decrease in the electron density on the BH groups [13] and hence a decrease in their hydride character.…”
mentioning
confidence: 99%