Planarity is one of the essential requirements for fluorescence in Red Fluorescent Protein chromophore analogs
暂无分享,去创建一个
[1] Jian Zhang,et al. Impact of π-Conjugation Length on the Excited-State Dynamics of Star-Shaped Carbazole-π-Triazine Organic Chromophores. , 2022, The journal of physical chemistry. A.
[2] S. Chandrasekar,et al. Synthesis, XRD, Hirshfeld surface analysis, ESP, HOMO-LUMO, Quantum chemical modeling and Anticancer activity of di(p-methyl benzyl)(dibromo)(1,10-phenanthroline) tin(IV) complex , 2022, Inorganic Chemistry Communications.
[3] Yuliang Jiang,et al. A Novel Coumarin-based Fluorescent Probe with Aggregation Induced Emission for Detecting CN− and its Applications in Bioimaging , 2021, Journal of Fluorescence.
[4] M. J. Turner,et al. CrystalExplorer: a program for Hirshfeld surface analysis, visualization and quantitative analysis of molecular crystals , 2021, Journal of applied crystallography.
[5] W. Qi,et al. Green fluorescent protein inspired fluorophores. , 2020, Advances in colloid and interface science.
[6] Ian D. Williams,et al. Why Are Twisted Molecules Nonluminescent in Solution , 2019 .
[7] J. Rocha,et al. Tunable Color of Aggregation-Induced Emission Enhancement in a Family of Hydrogen-Bonded Azines and Schiff Bases. , 2018, Chemistry.
[8] Xinyuan Zhu,et al. Emission enhancement and application of synthetic green fluorescent protein chromophore analogs , 2017 .
[9] W. Duan,et al. Microwave assisted solvent-free CH amination by silica-supported manganese dioxide , 2016 .
[10] Debashree Ghosh,et al. Effects of the benzoxazole group on green fluorescent protein chromophore crystal structure and solid state photophysics , 2016 .
[11] B. K. Rajbongshi,et al. Introduction of an electron push-pull system yields a planar Red Kaede fluorescence protein chromophore analogue stabilized by a C = O…π interaction , 2015, Journal of Chemical Sciences.
[12] R. Misra,et al. Unsymmetrical Donor-Acceptor-Acceptor-π-Donor Type Benzothiadiazole-Based Small Molecule for a Solution Processed Bulk Heterojunction Organic Solar Cell. , 2015, ACS applied materials & interfaces.
[13] Richard J. Gildea,et al. The anatomy of a comprehensive constrained, restrained refinement program for the modern computing environment – Olex2 dissected , 2015, Acta crystallographica. Section A, Foundations and advances.
[14] G. Sheldrick. SHELXT – Integrated space-group and crystal-structure determination , 2015, Acta crystallographica. Section A, Foundations and advances.
[15] B. K. Rajbongshi,et al. Tuning of intermolecular interactions results in packing diversity in imidazolin-5-ones , 2014, Journal of Chemical Sciences.
[16] M. Nethaji,et al. Segregation into Chiral Enantiomeric Conformations of an Achiral Molecule by Concomitant Polymorphism , 2012 .
[17] Wenjiao Song,et al. Fluorescence Imaging of Cellular Metabolites with RNA , 2012, Science.
[18] Guisheng Zhang,et al. C⋯π interaction of non-hydrogen bond type , 2012 .
[19] A. Sikder,et al. A DFT study of aminonitroimidazoles , 2012, Journal of Molecular Modeling.
[20] K. Saravanan,et al. Physiochemical properties of organic nonlinear optical crystal from combined experimental and theoretical studies. , 2011, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
[21] T. Xavier,et al. Vibrational spectra and DFT study of anticancer active molecule 2-(4-Bromophenyl)-1H-benzimidazole by normal coordinate analysis. , 2011, Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy.
[22] B. K. Rajbongshi,et al. Dominant π…π interaction in the self assemblies of 4-benzylidene imidazolin-5-one analogues , 2009 .
[23] Richard J. Gildea,et al. OLEX2: a complete structure solution, refinement and analysis program , 2009 .
[24] Dylan Jayatilaka,et al. Hirshfeld surface analysis , 2009 .
[25] M. Davidson,et al. Advances in fluorescent protein technology , 2007, Journal of Cell Science.
[26] M. Spackman,et al. Towards quantitative analysis of intermolecular interactions with Hirshfeld surfaces. , 2007, Chemical communications.
[27] J. Lippincott-Schwartz,et al. Imaging Intracellular Fluorescent Proteins at Nanometer Resolution , 2006, Science.
[28] K. Solntsev,et al. Solvatochromism of the green fluorescence protein chromophore and its derivatives. , 2006, Journal of the American Chemical Society.
[29] Sarit S. Agasti,et al. Solvent free Lewis acid catalyzed vinylogous condensation , 2006 .
[30] G. Savitha,et al. C–H⋯O interactions are favoured in the crystal structures of imidazolin-5-ones , 2005 .
[31] G. Savitha,et al. Short CO⋯C intermolecular contacts for molecular assembly , 2004 .
[32] Atsushi Miyawaki,et al. Photo-induced peptide cleavage in the green-to-red conversion of a fluorescent protein. , 2003, Molecular cell.
[33] J. Lippincott-Schwartz,et al. Development and Use of Fluorescent Protein Markers in Living Cells , 2003, Science.
[34] A. Miyawaki,et al. An optical marker based on the UV-induced green-to-red photoconversion of a fluorescent protein , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[35] K. Lukyanov,et al. Diversity and evolution of the green fluorescent protein family , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[36] M. Zimmer,et al. Green fluorescent protein (GFP): applications, structure, and related photophysical behavior. , 2002, Chemical reviews.
[37] A. Becke. Density-functional thermochemistry. III. The role of exact exchange , 1993 .
[38] Christopher A. Hunter,et al. The nature of .pi.-.pi. interactions , 1990 .
[39] R. Tsien. Fluorescent probes of cell signaling. , 1989, Annual review of neuroscience.
[40] Timothy Clark,et al. Efficient diffuse function‐augmented basis sets for anion calculations. III. The 3‐21+G basis set for first‐row elements, Li–F , 1983 .
[41] P. C. Hariharan,et al. The influence of polarization functions on molecular orbital hydrogenation energies , 1973 .
[42] J. R. Waters,et al. Quantum efficiency of Cypridina luminescence, with a note on that of Aequorea† , 1962 .