2001
DOI: 10.1039/b008424g
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Structure and properties of novel M(dmit)2 salts with the Me3N+­TEMPO cation radical (Me3N+­TEMPO = N,N,N­trimethyl(1­oxyl­2,2,6,6­tetramethylpiperidin­4­yl)ammonium)

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Cited by 36 publications
(28 citation statements)
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“…Therefore many researchers have introduced organic radicals in organic conducting salts. For example, charge-transfer (CT) salts of free radical substituted organochalcogen donors [7][8][9][10][11][12][13][14][15][16], CT complexes of free radicals and acceptors [17][18], CT salts of free radical substituted cations and acceptors [19][20][21][22][23], have been reported.…”
mentioning
confidence: 99%
“…Therefore many researchers have introduced organic radicals in organic conducting salts. For example, charge-transfer (CT) salts of free radical substituted organochalcogen donors [7][8][9][10][11][12][13][14][15][16], CT complexes of free radicals and acceptors [17][18], CT salts of free radical substituted cations and acceptors [19][20][21][22][23], have been reported.…”
mentioning
confidence: 99%
“…These values are similar to that obtained for the salt with the octahedral PF 6 À anion (y ¼ À0.2 K) and much weaker than that in (Me 3 N-TEMPO)I salt (y ¼ À6.3 K). (Me 3 N-TEMPO)ClO 4 was found to be isostructural (Figure 1; Pnma, a ¼ 11.170(5) Å , b ¼ 10.650(5) Å , c ¼ 13.264 (5) Å ), and shows similar antiferromagnetic-coupled chain (2J=k B ¼ À0.24 K) as in with (Me 3 N-TEM-PO)PF 6 (a ¼ 11.400(1) Å , b ¼ 10.852(1) Å , c ¼ 13.354 (2) Å ; 2J=k B ¼ À0.26 K) [6].…”
mentioning
confidence: 81%
“…The Me 3 N þ -TEMPO salts with X ¼ I À and PF 6 À show different structure and magnetic properties, i.e., both antiferromagnetic but strongly coupled dimer for (Me 3 N-TEMPO)I, weakly coupled chain for (Me 3 N-TEMPO)PF 6 [6]. Thus, solid-state properties of these salts can be controlled by a chemical modification of its counter anion, which can be readily available by metathesis reaction of (Me 3 N-TEMPO)I with the potassium or silver salt of the corresponding anion.…”
Section: Me 3 N 1 -Tempomentioning
confidence: 99%
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“…Namely, TEMPO radicals or verdazyl radicals act as donors to form CT complexes, which are isolated as solid substances. [11] A relatively high room-temperature conductivity has been found in the 1:1 salt with [Ni(dmit) 2 ], the 1:2 salt with [Ni(dmit) 2 ], and the 1:4 salt with [Pd(dmit) 2 ] (where dmit is 1,3-dithiole-2-thione-4,5-dithiolate) ranging from 4 10 ±3 S cm ±1 for the former salt to about 1 10 ±2 S cm ±1 for the latter two salts. [10] The electrical conductivity observed in each CT complex at room temperature ranges from 1.40 10 ±2 S cm ±1 to 3.95 10 ±5 S cm ±1 , which is in sharp contrast to other aminoxyl-based CT complexes, which have conductivities below 10 ±6 S cm ±1 .…”
Section: Organic Spin Systems With Carrier Transport Propertiesmentioning
confidence: 99%