2001
DOI: 10.1021/ic010630h
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Silver(I) Coordination Polymer of 2,5-Bis- (4‘,5‘-bis(methylthio)-1‘,3‘-dithiol-2‘-ylidene)- 1,3,4,6-tetrathiapentalene (TTM-TTP) and Its Highly Conductive Iodine Derivative

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Cited by 47 publications
(27 citation statements)
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“…The molecules 4-ethynyl-1,2-bis(methylthio)benzene and 4-ethynylmethylthiobenzene were prepared following a previously reported procedure. 18,44 Solution 1 H and 13 C NMR spectra were recorded on a 300 MHz Varian YH300 superconducting-magnet high-field NMR spectrometer at room temperature, with tetramethylsilane (TMS) as the internal standard. Except for 6, which was studied on an Oxford Gemini S Ultra diffractometer, all single crystal XRD analyses (data collection, structure solution and refinement) were performed on a Bruker AXS SMART APEX CCD system using MoKa (l = 0.71073 A ˚) radiation at 100(2) K. The structures were solved and refined by full-matrix least-squares on F o 2 using SHELXL 6.14 (see also Tables 1 and 2).…”
Section: General Proceduresmentioning
confidence: 99%
See 1 more Smart Citation
“…The molecules 4-ethynyl-1,2-bis(methylthio)benzene and 4-ethynylmethylthiobenzene were prepared following a previously reported procedure. 18,44 Solution 1 H and 13 C NMR spectra were recorded on a 300 MHz Varian YH300 superconducting-magnet high-field NMR spectrometer at room temperature, with tetramethylsilane (TMS) as the internal standard. Except for 6, which was studied on an Oxford Gemini S Ultra diffractometer, all single crystal XRD analyses (data collection, structure solution and refinement) were performed on a Bruker AXS SMART APEX CCD system using MoKa (l = 0.71073 A ˚) radiation at 100(2) K. The structures were solved and refined by full-matrix least-squares on F o 2 using SHELXL 6.14 (see also Tables 1 and 2).…”
Section: General Proceduresmentioning
confidence: 99%
“…1 H NMR (300 MHz, CDCl 3 ): d 2.48 (s, 12H), 7.14 (s, 16H), 7.45 (s, 2H). 13 (7). In a nitrogen-filled glovebox, L7 (5.0 mg, 8.8 mmol) and BiBr 3 (30.0 mg, 66.9 mmol) were loaded into a heavy-wall borosilicate glass tube, and benzene (0.4 mL, anhydrous) was added.…”
Section: 35-tri(4-methylthiophenyl)benzene (L6)mentioning
confidence: 99%
“…Silver(I) complexes have been applied in various fields, therefore, attracting great attention due to their structural features and functional considerations [1][2][3]. They have been tested as fluorescent materials [4], semiconductors [5,6], source of nanomaterials [7] and biological imaging agents [8] due to their interesting and fascinating physicochemical properties. Ag(I) complexes have also shown potential medical applications, most especially as antibacterial [9,10], antifungal [11], anticancer [12], and antimalarial agents [13].…”
Section: Introductionmentioning
confidence: 99%
“…Crystal engineering of coordination polymers attracts increased attention in the field of materials science because of their exceptional chemical and physical properties, such as magnetic [1][2][3] and conductive [4][5][6][7][8][9][10][11][12][13][14][15][16][17], dielectric [18][19][20], gas-absorbing [21][22][23], and catalytic properties [24][25][26][27]. In particular, mixed-valence coordination polymers have attracted considerable interest as a new class of functional materials because of their unique infinite structures and electronic states formed by the combination of different metal ions having versatile coordination architectures and a variety of organic bridging ligands.…”
Section: Introductionmentioning
confidence: 99%