Abstract

The novel tetrahedral 10-(4-carboxyphenyl)-2,8-diethyl-5,5-difluoro-1,3,7,9-tetramethyl-5H-di-pyrrolo[1,2-c:2’,1’-f][1,3,2]diazaborinin-4-ium-5-uide [NՈNBF2] BODIPY complex was prepared in a very good yield and via one-pot synthesis. The desired [NՈNBF2] has been used as a model complex for XRD/HSA interactions and DFT/B3LYP/6-311G(d,p) computations. The tetrahedral geometry around the boron center was demonstrated by DFT optimization and XRD-crystallography. The 1H, 11B, and 19F-NMR spectra were used also to support the high symmetrical BODIPY via π-extended phenomena. Moreover, the values of the DFT-calculated structural bond lengths/angles and DFT-IR were matched to the corresponding experimental XRD and IR parameters, respectively. The crystal lattice interactions were correlated to Hirshfeld surface analysis (HSA) calculations. Calculations of the Mulliken Atomic Charge (MAC), Natural Population Analysis (NPA), Global reactivity descriptors (GRD), and Molecular Electrostatic Potential (MEP) quantum parameters were performed to support the XRD/HSA interactions result. Analysis of the predicted Density of States (DOS), molecular orbital, and time-dependent density functional theory (TD-DFT) calculations have been combined to explain the experimental UV-vis spectra and electron transfer behavior in [NՈNBF2] complex using MeOH and other four solvents.

Highlights

  • There has been a rapid growth of new preparation strategies for the functionalization of B-complexes to enable binding to a biological target in order to change its optical properties; these strategies include cross-coupling reaction, halogenation, and nucleophilic aromatic substitution on the dipyrromethene part [6,7,8]

  • Well The as their varied applications is such as biological labels, tunable laserofdyes, probes, ongoing accommodation explicit from the considerable number articles being photoactive, photovoltaic devices, fluorescent nanocars, light-emitting devices, photoacreported about the synthesis and characterization of boron with dipyrromethene ligands (BODIPY) boron complexes as well tivatable compounds, energysuch transfer, triplet photosensitizers, PDT, photocatalytic reacas their varied applications as biological labels, tunable laser dyes, probes, photoactions, triplet–triplet annihilation up-conversion, and photo-induced production tive, photovoltaic devices, fluorescent nanocars, light-emitting devices, photoactivatable

  • The desired [N∩NBF2 ] complex was synthesized according to the reported method [30]

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Summary

A DFT and TD-DFT Study

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Introduction
Computational
Materials
XRD-Structure
Preparation and NMR
XRD and DFT
XRD Packing and HSA Investigation
FT-IR and DFT-IR Spectroscopy
Conclusions
Full Text
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