Spectroscopic studies of synthesized coumarins
P. K. Ingalagondi, Omnath Patil, T. Sankarappa, S.M. Hanagodimath
Abstract
P. K. Ingalagondi, Omnath Patil, T. Sankarappa, S.M. Hanagodimath
Abstract
The ground state (µg) and excited state (µe) dipole moments of newly synthesized coumarins namely 1-(2-Methoxy-phenoxymethyl)-benzo[f]chromen-3-one (2-MPBC) and 1-(3-Methoxy-phenoxymethyl)-benzo[f]chromen-3-one (3-MPBC) were estimated at room temperature in solvents of different polarities. The excited state dipole moments were estimated using Solvatochromic shift method. It was observed that the excited state dipole moments estimated by solvatochromic shift method were larger than the ground state dipole moments, which indicates that the excited state is more polar than the ground state.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The ground state (µg) and excited state (µe) dipole moments of newly synthesized coumarins namely 1-(2-Methoxy-phenoxymethyl)-benzo[f]chromen-3-one (2-MPBC) and 1-(3-Methoxy-phenoxymethyl)-benzo[f]chromen-3-one (3-MPBC) were estimated at room temperature in solvents of different polarities. The excited state dipole moments were estimated using Solvatochromic shift method. It was observed that the excited state dipole moments estimated by solvatochromic shift method were larger than the ground state dipole moments, which indicates that the excited state is more polar than the ground state.
Key concepts: Solvatochromism, Excited state, Dipole, Ground state, Chemistry, Bond dipole moment, Chemical polarity, Atomic physics