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88150

四硫富瓦烯

Name: 四硫富瓦烯
Brand: SIAL

purum, ≥98.0% (HPLC)

别名:

Δ2,2′-双-1,3-二硫杂环戊二烯, TTF

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经验公式（希尔记法）:

C₆H₄S₄

化学文摘社编号:

31366-25-3

分子量:

204.36

EC Number:

250-593-7

UNSPSC Code:

12352103

MDL number:

MFCD00005492

Beilstein/REAXYS Number:

1617956

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grade

purum

assay

≥98.0% (HPLC)

mp

116-119 °C

SMILES string

S1C=CS\C1=C2/SC=CS2

InChI

1S/C6H4S4/c1-2-8-5(7-1)6-9-3-4-10-6/h1-4H

InChI key

FHCPAXDKURNIOZ-UHFFFAOYSA-N

法规信息

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分析证书(COA)

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Formation of self-assembled chains of tetrathiafulvalene on a Cu(100) surface.

Yang Wang et al.

The journal of physical chemistry. A, 115(45), 13080-13087 (2011-10-01)

Formation of self-assembled chains of tetrathiafulvalene (TTF) on the Cu(100) surface has been investigated by scanning tunneling microscopy and density functional theory calculations that include semiempirical van der Waals (vdW) interaction corrections. The calculations show that the chain structures observed

Tetrathiafulvalene-fused porphyrins via quinoxaline linkers: symmetric and asymmetric donor-acceptor systems.

Hongpeng Jia et al.

Chemphyschem : a European journal of chemical physics and physical chemistry, 13(14), 3370-3382 (2012-07-04)

A tetrathiafulvalene (TTF) donor is annulated to porphyrins (P) via quinoxaline linkers to form novel symmetric P-TTF-P triads 1 a-c and asymmetric P-TTF dyads 2 a,b in good yields. These planar and extended π-conjugated molecules absorb light over a wide region of

High nuclearity complexes of lanthanide involving tetrathiafulvalene ligands: structural, magnetic, and photophysical properties.

Fabrice Pointillart et al.

Inorganic chemistry, 52(3), 1610-1620 (2013-01-18)

The reaction between the tetrakis(2-pyridyl-N-oxidemethylthio)tetrathiafulvalene ligand (L) and Ln(hfac)(3)·2H(2)O precursors (where hfac(-) = 1,1,1,5,5,5-hexafluoroacetylacetonate anion and Ln = Tb(III) (1), Dy(III) (2), Er(III) (3), and Yb(III) (4) and (4b)) leads to the formation of five tetranuclear complexes of formula [Ln(4)(hfac)(12)(L)(2)](n)·xCHCl(3)·yC(6)H(14)

Metal-ion-promoted electron transfer between tetrathiafulvalene and quinone units within a calix[4]arene framework and tuning through coordination of the neighboring crown ether with a sodium cation.

Fei Sun et al.

Chemistry, an Asian journal, 7(1), 183-189 (2011-10-06)

A new calix[4]arene 1 with tetrathiafulvalene (TTF), quinone, and crown ether units in the lower rim was designed and synthesized with the aim to investigate the possibility to tune the metal-ion promoted electron transfer by coordination of the crown ether

Spontaneous redox synthesis of the charge transfer material TTF4[SVMo11O40].

Qi Li et al.

Inorganic chemistry, 51(23), 12929-12937 (2012-11-14)

The charge-transfer material TTF-SV(IV)Mo(11)O(40) (TTF = tetrathiafulvalene) was prepared by a spontaneous redox reaction between TTF and the vanadium-substituted polyoxometalate (n-Bu(4)N)(3)[SV(V)Mo(11)O(40)] in both solution and solid state phases. Single crystal X-ray diffraction gave the stoichiometry TTF(4)[SVMo(11)O(40)]·2H(2)O·2CH(2)Cl(2), with the single V

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