Synthesis and Spectral Properties of tert-Butyl-Substituted Triisoindodimethene and Its Boron Complexes

2021 ◽  
Vol 57 (10) ◽  
pp. 1614-1620
Author(s):  
A. I. Koptyaev ◽  
T. A. Rumyantseva ◽  
D. V. Tyurin ◽  
V. E. Maizlish ◽  
V. V. Aleksandriiskii ◽  
...  
2011 ◽  
Vol 15 (01) ◽  
pp. 54-65 ◽  
Author(s):  
Ekaterina S. Taraymovich ◽  
Andrey B. Korzhenevskii ◽  
Yulia V. Mitasova ◽  
Roman S. Kumeev ◽  
Oscar I. Koifman ◽  
...  

Starting from easily available thiophenols (PhSH (1a), 4-tert-butyl-PhSH (1b)) and oxalylchloride we have prepared 2,3-thianaphtenequinones 2a,b which were then successively converted to thianaphthene-2,3-dicarboxylic acids 4a,b their imides 10a,b, diamides 9a,b and finally to thianaphthene-2,3-dicarbonitriles 11a,b — the key precursors for the series of novel porphyrazines bearing four 2,3-annulated thianaphthene moieties. The free-bases 12a,b were obtained by cyclotetramerization of the dinitrile 11a,b in the presence of lithium in n-pentanol, while the reaction with magnesium(II) butoxide in n-butanol leads to the Mg(II) complex 13a. Complexes with Al(III) (14a,b), Ga(III) (14a,b) and In(III) (14a,b) were obtained by the template cyclotetramerization of the dinitriles 11a,b in a melt with the corresponding (hydroxy)acetates. Tetra(2,3-thianaphtheno)porphyrazine 12a and its metal complexes 13a–15a are only sparingly soluble in common organic solvents, the solubility is enhanced for their tert-butyl substituted derivatives 12b, 14b–16b. The study of the electronic absorbtion spectra has revealed that the extension of the porphyrazine π-chromophore by fusion of four thianaphthene fragments due to the angular type of their annulation (similar to that found in 1,2-naphthalocyanines) and negative inductive effect of the sulfur atoms has an effect on its spectral properties which is less than in the case of the isoelectronic naphthalene rings fusion and is comparable with the influence of four benzene rings in phthalocyanines.


2019 ◽  
Vol 89 (4) ◽  
pp. 727-735 ◽  
Author(s):  
A. S. Burlov ◽  
S. B. Zaichenko ◽  
L. D. Popov ◽  
V. G. Vlasenko ◽  
G. S. Borodkin ◽  
...  

2008 ◽  
Vol 78 (8) ◽  
pp. 1622-1625
Author(s):  
S. V. Efimova ◽  
A. B. Korzhenevskii ◽  
O. I. Koifman

1996 ◽  
Vol 74 (4) ◽  
pp. 508-515 ◽  
Author(s):  
Svetlana V. Kudrevich ◽  
Johan E. Van Lier ◽  
Maria G. Galpern ◽  
Evgeny A. Luk'yanets

Several derivatives of 2,3-dicyanopyrazine were prepared via the condensation of o-quinones with diaminomaleodinitrile. Benzo[f]quinoxaline-2,3-dinitrile was obtained from 1,2-naphthoquinone, and a series of isomeric, di-tert-butyl substituted 5,6-(9,10-phenanthro)-2,3-dicyanopyrazines were prepared from the corresponding di-tert-butyl-9,10-phenanthrenequinones. Complexation of benzo[f]quinoxaline-2,3-dinitrile, and unsubstituted 5,6-(9,10-phenanthro)-2,3-dicyanopyrazine, with an appropriate metal salt yielded metal complexes of tetra-2,3-(benzo[f]quinoxalino)porphyrazine and tetra-2,3-[5,6-(9,10-phenanthro)]porphyrazine, respectively. Metal-free tetra-2,3-[5,6-(9,10-phenanthro)porphyrazine was obtained from the dilithium derivative by demetallation in HCl. These compounds have limited solubility in organic solvents, such as quinoline, and are aggregated in solutions. To eliminate the aggregation phenomenon and to determine the spectral properties of angularly annelated naphthalocyanine aza analogs, we prepared several isomeric tetra-2,3-[5,6-(di-tert-butyl-9,10-phenanthro)pyrazino]porphyrazines. These octa(tert-butyl) substituted complexes were synthesized via complexation of di-tert-butyl substituted 5,6-(9,10-phenanthro)-2,3-dicyanopyrazines with metal salts in the presence of urea, quinoline, and tri(n-butyl)amine, and purified by silica gel chromatography. They are soluble in chloroform and substantially monomerized in solutions. A hypsochromic shift of the Q-band of octaaza naphthalocyanines versus their carbocyclic analogs was observed for all aza analogs, with the extent of the shift depending on the composition of the aromatic macrocycle. Thus, the first angularly annelated benzo ring addition causes a hypsochromic shift (∼25 nm) of the Q-band of tetra-2,3-quinoxalinoporphyrazine, whereas addition of a second condensed benzo ring has little effect. Key words: phthalocyanine, aza analog, tetra-2,3-quinoxalinoporphyrazine, angular annelation.


Author(s):  
Pavel A. Tarakanov ◽  
Anton O. Simakov ◽  
Alexandr Yu. Tolbin ◽  
Irina O. Balashova ◽  
Vladimir I. Shestov ◽  
...  

ChemInform ◽  
1987 ◽  
Vol 18 (40) ◽  
Author(s):  
I. V. SHCHERBAKOVA ◽  
E. V. KUZNETSOV ◽  
L. YU. UKHIN ◽  
M. D. GHEORGHIU ◽  
A. MEGHEA ◽  
...  

2013 ◽  
Vol 17 (08n09) ◽  
pp. 785-790 ◽  
Author(s):  
Elena A. Makarova ◽  
Semyon V. Dudkin ◽  
Evgeny A. Lukyanets

An efficient synthetic route for the preparation of benzene or 1,2-naphthalene fused and phenyl substituted metal-free tetraazachlorins with yields up to 40% was developed using In ( III ) as a removable template. New substituted tribenzotetraazachlorins derivatives with tert-butyl and phenylsulfanyl groups in β and α position of fused benzene rings, correspondingly, were synthesized by novel approach and their spectral properties were investigated.


Sign in / Sign up

Export Citation Format

Share Document