Relevant bibliographies by topics / BODIPY based zwitterionic molecules

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Academic literature on the topic 'BODIPY based zwitterionic molecules'

Author: Grafiati
Published: 18 May 2024

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Journal articles on the topic "BODIPY based zwitterionic molecules"

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Sutradhar, Tanushree, and Anirban Misra. "The role of π-linkers and electron acceptors in tuning the nonlinear optical properties of BODIPY-based zwitterionic molecules." RSC Advances 10, no. 66 (2020): 40300–40309. http://dx.doi.org/10.1039/d0ra02193h.

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Das, Sarasija, Sudipto Dey, Sanujit Patra, Arindam Bera, Totan Ghosh, Bibin Prasad, Kapil Dev Sayala, Krishnendu Maji, Anjan Bedi, and Sashi Debnath. "BODIPY-Based Molecules for Biomedical Applications." Biomolecules 13, no. 12 (November 30, 2023): 1723. http://dx.doi.org/10.3390/biom13121723.

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BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) derivatives have attracted attention as probes in applications like imaging and sensing due to their unique properties like (1) strong absorption and emission in the visible and near-infrared regions of the electromagnetic spectrum, (2) strong fluorescence and (3) supreme photostability. They have also been employed in areas like photodynamic therapy. Over the last decade, BODIPY-based molecules have even emerged as candidates for cancer treatments. Cancer remains a significant health issue world-wide, necessitating a continuing search for novel therapeutic options. BODIPY is a flexible fluorophore with distinct photophysical characteristics and is a fascinating drug development platform. This review provides a comprehensive overview of the most recent breakthroughs in BODIPY-based small molecules for cancer or disease detection and therapy, including their functional potential.
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Gayathri, Thumuganti, Ravulakollu Srinivasa Rao, Vinay Gupta, and Surya Prakash Singh. "Panchromatic aza-Bodipy based π-conjugates." New Journal of Chemistry 45, no. 17 (2021): 7792–98. http://dx.doi.org/10.1039/d1nj00847a.

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Squeo, Benedetta Maria, Lucia Ganzer, Tersilla Virgili, and Mariacecilia Pasini. "BODIPY-Based Molecules, a Platform for Photonic and Solar Cells." Molecules 26, no. 1 (December 31, 2020): 153. http://dx.doi.org/10.3390/molecules26010153.

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The 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY)-based molecules have emerged as interesting material for optoelectronic applications. The facile structural modification of BODIPY core provides an opportunity to fine-tune its photophysical and optoelectronic properties thanks to the presence of eight reactive sites which allows for the developing of a large number of functionalized derivatives for various applications. This review will focus on BODIPY application as solid-state active material in solar cells and in photonic devices. It has been divided into two sections dedicated to the two different applications. This review provides a concise and precise description of the experimental results, their interpretation as well as the conclusions that can be drawn. The main current research outcomes are summarized to guide the readers towards the full exploitation of the use of this material in optoelectronic applications.
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Gupta, Monika, Soumyaditya Mula, Mrityunjay Tyagi, Tapan K. Ghanty, Sushant Murudkar, Alok K. Ray, and Subrata Chattopadhyay. "Rational Design of Boradiazaindacene (BODIPY)-Based Functional Molecules." Chemistry - A European Journal 19, no. 52 (November 28, 2013): 17766–72. http://dx.doi.org/10.1002/chem.201302359.

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Ma, Guanglong, Weifeng Lin, Zhen Wang, Juan Zhang, Haofeng Qian, Liangbo Xu, Zhefan Yuan, and Shengfu Chen. "Development of polypeptide-based zwitterionic amphiphilic micelles for nanodrug delivery." Journal of Materials Chemistry B 4, no. 31 (2016): 5256–64. http://dx.doi.org/10.1039/c6tb01144f.

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Rybczynski, Patryk, and Anna Kaczmarek-Kȩdziera. "BODIPY dimers: structure, interaction, and absorption spectrum." Structural Chemistry 32, no. 3 (March 26, 2021): 953–65. http://dx.doi.org/10.1007/s11224-021-01759-1.

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AbstractThe object of the present study are BODIPY molecules obtained previously by Piskorz et al. (Dyes Pigm. 178:108322, 2020) for their antimicrobial activity. Structural analysis of the BODIPY dimers is presented in context of the aggregation influence on the photophysical properties. The thorough investigation of the nature of intermolecular interaction in the representative BODIPY dimers is provided together with the decomposition of the interaction energy into the components of well-defined origin according to SAPT procedure. For the model BODIPY systems the careful examination of the interaction nature for the dimer structure based on experimental crystal study as well as fully optimized is given. The tendencies observed in the model dimers are further on investigated for two pairs of BODIPY systems designed for biomedical application. The analyzed molecules are shown to maximize the mutual interaction by the optimization of the stacking dispersion contacts between the aromatic rings of the molecules, therefore producing stable dimers. The estimation of SAPT0 interaction energy components confirms the dominating dispersion character arising from mutual BODIPY core contacts. The influence of the dimerization process on the photophysical properties of the systems studied theoretically depends to the high extend on the dimerization mode and is significant for parallel and antiparallel dispersion-governed dimers.
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Sabari, P., Rima Sengupta, B. Umasekhar, and Mangalampalli Ravikanth. "Meso-pyrrolyl BODIPY based colorimetric optical sensor for Cu2+ ions." Journal of Porphyrins and Phthalocyanines 24, no. 09 (August 28, 2020): 1121–28. http://dx.doi.org/10.1142/s1088424620500261.

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A simple meso-pyrrolyl BODIPY-Schiff base conjugate was synthesized by reacting ([Formula: see text]-formylpyrrolyl) BODIPY with 2-aminophenol in ethanol at reflux followed by recrystallization from CH2Cl2/petroleum ether, affording the conjugate in 72% yield. The conjugate was thoroughly characterized by HR-MS, 1D and 2D NMR and X-ray crystallographic techniques. The X-ray structure of the meso-pyrrolyl BODIPY-Schiff base conjugate revealed that the meso-pyrrole and the phenyl substituents were deviated by an angle of [Formula: see text] and [Formula: see text], respectively, from the plane of the BF2-dipyrrin core. The absorption spectrum of the conjugate was similar to the ([Formula: see text]-formylpyrrolyl) BODIPY with a strong absorption band at 508 nm, whereas the fluorescence of the ([Formula: see text]-formylpyrrolyl) BODIPY was completely quenched in the BODIPY-Schiff base conjugate. Furthermore, cation sensing studies revealed that the conjugate has a specific sensing ability for the Cu(II) ion even in the presence of the other metal ions, as verified by the visual, absorption and mass spectral studies. The DFT optimized structure revealed that the Cu(II) ion was bound to pyrrolic nitrogen, imine nitrogen, phenolic oxygen and two water molecules in a distorted square pyramidal fashion. TD-DFT studies accounted well for the absorption spectra of the BODIPY-Schiff base conjugate and its Cu[Formula: see text] bound complex.
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Demirel Topel, Seda, and Mustafa İlker Beyaz. "Fluorescence quenching-based bodipy-boronic acid linked viologen dual system for potential glucose sensing applications." Sensor Review 42, no. 1 (October 28, 2021): 62–69. http://dx.doi.org/10.1108/sr-03-2021-0088.

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Purpose The purpose of this study is to develop a non-enzymatic based glucose-sensing platform composed of Bodipy-BBV dual system which can be monitored by a photodetector under the blue LED excitation. Design/methodology/approach The sensor has been developed from a dual system including a fluorescent dye, an aldehyde derivative of boron dipyrromethene (Bodipy) and a quencher, orto-boronic acid linked viologen (o-BBV) where their combination resulted in a ratiometric fluorescence quenching in ethanol: PBS (1:1, pH:7.4) solution under UV light excitation. By glucose addition, o-BBV has been released from the Bodipy and binded to cis-diol groups of glucose, thereby fluorescence emission of Bodipy has been regained. Furthermore, a setup consisting of a light emitting diode (LED) and a photodiode (PD) was used to prove electrical detection of glucose without the need for expensive and bulky optical equipment, enabling the development of a miniaturized and low-cost glucose-sensing platform. Findings The fluorescence intensity of the Bodipy derivative in the solution (2 × 10−6 M) was diminished by 93% in the presence of o-BBV solution (5 × 10−3 M). Upon the glucose addition, 81% of the Bodipy fluorescence intensity has been recovered after introduction of 30 mM of glucose, where the ratio of o-BBV/Bodipy was 35:1. A linear response between 10 and 30 mM glucose concentration was obtained, which covers the biologically significant range. A high correlation between the photodiode current and Bodipy fluorescence intensity was achieved. Originality/value Even though Bodipy molecules are known with their superior optical properties and applied to the fluorescence-based detection of glucose, to the best of the authors’ knowledge, no work has been reported on Bodipy-BBV dual system to detect glucose molecules as a non-enzymatic based method. This design enables the dye and the quencher to independently coexist in the solution, allowing for tuning of their individual concentrations to optimize the glucose sensitivity. Furthermore, an electrical light detection scheme consisting of a LED and a photodiode has been implemented to eliminate the bulky optical equipment from the measurement setup and further this work for the development of a compact and inexpensive sensor. The results presented here demonstrate the feasibility of this system for the development of a novel glucose sensor.
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Nisanci, Bilal, Sinem Sahinoglu, Esra Tuner, Mustafa Arik, İbrahim Kani, Arif Dastan, and Özgür Altan Bozdemir. "Synthesis of an F-BODIPY [2]catenane using the chemistry of bis(dipyrrinato)metal complexes." Chemical Communications 53, no. 92 (2017): 12418–21. http://dx.doi.org/10.1039/c7cc07021g.

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Dissertations / Theses on the topic "BODIPY based zwitterionic molecules"

1

Sutradhar, Tanushree. "Theoretical investigation on optoelectronic properties of nanoclusters and conjugates." Thesis, University of North Bengal, 2021. http://ir.nbu.ac.in/handle/123456789/4750.

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Singh, S. "BODIPY based small molecules and polymers for organic field effect transistors." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2016. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2259.

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Book chapters on the topic "BODIPY based zwitterionic molecules"

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Hall, Michael John, and Santiago de la Moya. "BODIPY Based Emitters of Circularly Polarized Luminescence." In Circularly Polarized Luminescence of Isolated Small Organic Molecules, 117–49. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2309-0_6.

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