Cesium dithiolate based syntheses of keto-functionalized thio-crown ethers employing the novel building block 1,3-dimercaptoacetone. Molecular structures of 2,5,9,12-tetrathia-7-oxo(13)-m-benzenophane and 1,4,7,10,13-pentathiacyclohexadecan-15-one. [Erratum to document cited in CA120:77269]

1994 ◽  
Vol 59 (11) ◽  
pp. 3242-3242
Author(s):  
Jilles J. H. Edema ◽  
Jan Buter ◽  
Franck S. Schoonbeek ◽  
Auke Meetsma ◽  
Fre van Bolhuis ◽  
...  
2014 ◽  
Vol 10 ◽  
pp. 714-721 ◽  
Author(s):  
Yuta Takano ◽  
Yuki Nagashima ◽  
M Ángeles Herranz ◽  
Nazario Martín ◽  
Takeshi Akasaka

The [4 + 2] cycloaddition of o-quinodimethanes, generated in situ from the sultine 4,5-benzo-3,6-dihydro-1,2-oxathiin 2-oxide and its derivative, to La metal-encapsulated fullerenes, La2@C80 or La@C82, afforded the novel derivatives of endohedral metallofullerenes (3a,b, 4a,b and 5b). Molecular structures of the resulting compounds were elucidated using spectroscopic methods such as MALDI–TOF mass, optical absorption, and NMR spectroscopy. The [4 + 2] adducts of La2@C80 (3a,b, and 4a,b) and La@C82 (5b), respectively, retain diamagnetic and paramagnetic properties, as confirmed by EPR spectroscopy. Dynamic NMR measurements of 4a at various temperatures demonstrated the boat-to-boat inversions of the addend. In addition, 5b revealed remarkable thermal stability in comparison with the reported [4 + 2] cycloadduct of pentamethylcyclopentadiene and La@C82 (6). These findings demonstrate the utility of sultines to afford thermodynamically stable endohedral metallofullerene derivatives for the use in material science.


2021 ◽  
Author(s):  
Haifen Liu ◽  
Zixuan Zhu ◽  
Huafeng Li ◽  
Weili Fan ◽  
Kaihua Ning ◽  
...  

Non-fullerene acceptors have received a great deal of attention over the past several years, and numerous modifications on the molecular structures significantly boosted the power conversion efficiencies (PCEs). To be...


1990 ◽  
Vol 45 (9) ◽  
pp. 1235-1242 ◽  
Author(s):  
Günter Schmid ◽  
Abdel K. Boutrid ◽  
Eva-Maria Kreuzer

The (1-tert-butyl-2-methyl-1 H-1,2-azaborolyl)cobalt fragment (AbCo), available from AbCo(C2H4)2 (1), serves as a building block in a series of complexes and clusters. The mononuclear complexes AbCo(C2H4)PMe3 (2), AbCo(PMe3)2 (3), AbCo(C2H4)P(OMe)3 (4), AbCo(P(OMe)3)2 (5), AbCo(C2H4)CO (6), and AbCo(CO)2 (7) are easily prepared from 1. AbCo(CpH) (8) is formed from 1 and CpCo(C2H4)2 together with AbCp3Co4H4 (9). The tetranuclear cluster Ab4Co4H4 (10) results, if 1 is warmed to 80 °C without a solvent. Ab3(CO)3Co3 (11) is available by a co-thermolysis of 1 and 7. Thermolysis of 6 leads to the trinuclear cluster Ab3(CO)2Co3 (12). Photolytical degradation of 7 forms the dinuclear complex Ab2(CO)3Co2 (13). Mass spectrometry, IR spectroscopy, and NMR investigations serve to elucidate the molecular structures.


Polyhedron ◽  
2010 ◽  
Vol 29 (3) ◽  
pp. 1069-1077 ◽  
Author(s):  
Ümmühan Ocak ◽  
Miraç Ocak ◽  
Aysel Başoğlu ◽  
Semanur Parlayan ◽  
Dilek Başaran ◽  
...  
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