Synthesis and characterization of (β-diketonato)silver complexes of 7-tert-butoxynorbornadiene. Single-crystal structures of (hfac) (7-But-O-NBD)Ag and [(hfac)2(7-But-O-NBD)Ag2]n

Polyhedron ◽  
1997 ◽  
Vol 16 (13) ◽  
pp. 2147-2154 ◽  
Author(s):  
Chi Kai-Ming ◽  
Chen Kuo-Hsien ◽  
Lin Hsiu-Chen ◽  
Lin Kuan-Jiuh
Polyhedron ◽  
2000 ◽  
Vol 19 (15) ◽  
pp. 1803-1807 ◽  
Author(s):  
Inamur Rahaman Laskar ◽  
Tapas Kumar Maji ◽  
Siddhartha Chaudhuri ◽  
Ashutosh Ghosh ◽  
Nirmalendu Ray Chaudhuri

Molecules ◽  
2020 ◽  
Vol 25 (14) ◽  
pp. 3162 ◽  
Author(s):  
Dalila Rocco ◽  
Alessandro Prescimone ◽  
Edwin C. Constable ◽  
Catherine E. Housecroft

The preparation and characterization of 4′-(4-n-octyloxyphenyl)-3,2′:6′,3″-terpyridine (8) and 4′-(4-n-nonyloxyphenyl)-3,2′:6′,3″-terpyridine (9) are reported. The single crystal structures of 4′-(4-n-hexyloxyphenyl)-3,2′:6′,3″-terpyridine (6), 4′-(4-n-heptyloxyphenyl)-3,2′:6′,3″-terpyridine (7), and compounds 8 and 9 have been determined. The conformation of the 3,2′:6′,3″-tpy unit is trans,trans in 6 and 7, but switches to cis,trans in 8 and 9. This is associated with significant changes in the packing interactions with a more dominant role for van der Waals interactions between adjacent n-alkyloxy chains and C–Hmethylene... π interactions in 8 and 9. The solid-state structures of 6 and 7 with the n-hexyloxy and n-heptyloxy chains feature interwoven sheets of supramolecular assemblies of molecules, with pairs of n-alkyloxy chains threaded through cavities in an adjacent sheet.


2018 ◽  
Vol 14 ◽  
pp. 1956-1960 ◽  
Author(s):  
Haiyan Guan ◽  
Mingbo Zhou ◽  
Bangshao Yin ◽  
Ling Xu ◽  
Jianxin Song

A π-extended “earring” subporphyrin 3 was synthesized from β,β′-diiodosubporphyrin and diboryltripyrrane via a Suzuki–Miyaura coupling and following oxidation. Its Pd complex 3Pd was also synthesized and both of the compounds were fully characterized by 1H NMR, MS and X-ray single crystal diffraction. The 1H NMR spectra and single crystal structures revealed that aromatic ring current did not extend to the “ear” in both of the two compounds. Their UV–vis/NIR spectra were recorded and the absorption of both compounds is extended to the NIR region and that the absorption of 3Pd is further red-shifted and more intense.


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