TY - JOUR
T1 - Hybrid Macrocycles of Subporphyrins and Triphyrins
AU - Kumar, Ankit
AU - Rajeswara Rao, M.
AU - Lee, Way Zen
AU - Ravikanth, Mangalampalli
N1 - Funding Information:
M.R. thanks the Science & Engineering Research Board, Government of India (EMR/2015/002196), for funding the project, and A.K. thanks UGC for the doctoral fellowship.
Publisher Copyright:
© 2017 American Chemical Society.
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.
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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 -