Abstract
The dibenzofuran/dibenzothiophene-based nonaromatic hybrid macrocycles, exhibiting the features of both contracted macrocycles, subporphyrins and triphyrins, have been synthesized under simple reaction conditions using readily available precursors. The monoanionic new macrocyclic ligands with three donor atoms, such as two pyrrole nitrogens and one dibenzofuran oxygen or dibenzothiophene sulfur, readily form Re(I) complexes.
| Original language | English |
|---|---|
| Pages (from-to) | 5924-5927 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 19 |
| Issue number | 21 |
| DOIs | |
| Publication status | Published - 2017 Nov 3 |
Fingerprint
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
Cite this
Hybrid Macrocycles of Subporphyrins and Triphyrins. / Kumar, Ankit; Rajeswara Rao, M.; Lee, Way-Zen; Ravikanth, Mangalampalli.
In: Organic Letters, Vol. 19, No. 21, 03.11.2017, p. 5924-5927.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Hybrid Macrocycles of Subporphyrins and Triphyrins
AU - Kumar, Ankit
AU - Rajeswara Rao, M.
AU - Lee, Way-Zen
AU - Ravikanth, Mangalampalli
PY - 2017/11/3
Y1 - 2017/11/3
N2 - The dibenzofuran/dibenzothiophene-based nonaromatic hybrid macrocycles, exhibiting the features of both contracted macrocycles, subporphyrins and triphyrins, have been synthesized under simple reaction conditions using readily available precursors. The monoanionic new macrocyclic ligands with three donor atoms, such as two pyrrole nitrogens and one dibenzofuran oxygen or dibenzothiophene sulfur, readily form Re(I) complexes.
AB - The dibenzofuran/dibenzothiophene-based nonaromatic hybrid macrocycles, exhibiting the features of both contracted macrocycles, subporphyrins and triphyrins, have been synthesized under simple reaction conditions using readily available precursors. The monoanionic new macrocyclic ligands with three donor atoms, such as two pyrrole nitrogens and one dibenzofuran oxygen or dibenzothiophene sulfur, readily form Re(I) complexes.
UR - http://www.scopus.com/inward/record.url?scp=85032979264&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85032979264&partnerID=8YFLogxK
U2 - 10.1021/acs.orglett.7b02919
DO - 10.1021/acs.orglett.7b02919
M3 - Article
AN - SCOPUS:85032979264
VL - 19
SP - 5924
EP - 5927
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 21
ER -