1997
DOI: 10.1039/a703603e
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Triple-decker naphthalene complex of thulium(iii); synthesis and molecular structure of [{Tm(dme)}2(η2-C10H8 )2(μ2-η4:η4- C10H8)]

Abstract: 2 [TmI 2 (dme) 3 ] + 4 LiC 10 H 8 dme, 20 °C [{Tm(dme)} 2 (C 10 H 8 ) 3 ] + 4 LiI + C 10 H 8 1, 92% C(11′) C(11) C(12) C(15) C(13) C(14) Tm O(2) C(19) C(18) C(17) O(1) C(16) C(4) C(3) C(2) C(1) C(10) C(5) C(6) C(9) C(8) C(7)

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Cited by 50 publications
(27 citation statements)
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“…These bond lengths are very close to those of the neutral naphthalene ligand in the anionic complex [(η 5 ‐Cp)V(C 10 H 8 )] − 15. 16 In comparison, the CC bond lengths of the coordinated arene unit in complexes that contain a dianionic naphthalene ligand, such as [CpV(C 10 H 8 )VCp],18 [CpLu(C 10 H 8 )(DME)],19 [(μ 2 ‐η 4 :η 4 ‐C 10 H 8 ){LaI 2 (THF) 3 } 2 ],20 and [Tm(DME) 2 (C 10 H 8 ) 3 ],21 show obvious long–short–long character. The naphthalene ligand in 3 is slightly bent, as in the anthracene ligand of complex 2 , with a fold angle of 14.0° at the central carbon atoms (C59 and C61) of the coordinating ring.…”
Section: Resultsmentioning
confidence: 99%
“…These bond lengths are very close to those of the neutral naphthalene ligand in the anionic complex [(η 5 ‐Cp)V(C 10 H 8 )] − 15. 16 In comparison, the CC bond lengths of the coordinated arene unit in complexes that contain a dianionic naphthalene ligand, such as [CpV(C 10 H 8 )VCp],18 [CpLu(C 10 H 8 )(DME)],19 [(μ 2 ‐η 4 :η 4 ‐C 10 H 8 ){LaI 2 (THF) 3 } 2 ],20 and [Tm(DME) 2 (C 10 H 8 ) 3 ],21 show obvious long–short–long character. The naphthalene ligand in 3 is slightly bent, as in the anthracene ligand of complex 2 , with a fold angle of 14.0° at the central carbon atoms (C59 and C61) of the coordinating ring.…”
Section: Resultsmentioning
confidence: 99%
“…However, for the next three years neither my lab nor the Bochkarev lab obtained any significant new reductive reactivity from this Tm 2+ complex [56,[58][59][60]61]. The intensely colored green compound reacted quickly with many substrates to give colorless Tm 3+ products, but TmI 3 was the only product readily identified.…”
Section: New Molecular Divalent Oxidation States In Solutionmentioning
confidence: 94%
“…The disproportionation process is dependent on the nature of both anion and cation. For instance, attempts of the exchange reaction between lithium naphthalenide, Li + (C 10 H 8 ) − and lanthanide halides in THF lead to the disproportionation of the radical anions of (C 10 H 8 ) − to the dianion (C 10 H 8 ) 2− and neutral naphthalene, affording solely lanthanide complexes with the naphthalene dianion 5be. Recently, Gambarotta, Budzelaar and co‐workers reported the formation and crystal structure of a trianion formed by reduction of α,α′‐diiminopyridine with lithium 7.…”
Section: Methodsmentioning
confidence: 99%