48. Perfluoroalkylfullerenes

      Boltalina, O. V., Kuvychko, I. V.; Popov A. A.; Shustova, N. B.; Strauss, S. H.

      Chem. Rev. 2015, 115, 1051–1105.

47. An Elusive Fulvene 1,7,11,24-C60(CF3)4 and Its Unusual Reactivity 

      Whitaker, J. B.; Kuvychko, I. V.; Shustova, N. B.; Chen, Y.-S.; Strauss, S. H.; Boltalina, O. V.

      Chem. Commun. 2014, 50, 1205–1208.

  1. 46.Selective Turn-On Ammonia Sensing Enabled by High-Temperature Fluorescence in Metal–Organic Frameworks with Open Metal Sites

      Shustova, N. B.; Cozzolino, A. F.; Reineke, S.; Baldo, M.; Dincă, M.  

      J. Am. Chem. Soc. 2013, 135, 13326–13329.

  1. 45.Regioselective Sequential Additions of Nucleophiles and Electrophiles to Perfluoroalkylfullerenes: Which Cage C Atoms Are the Most Reactive and Why?

      Clikeman, T. T.; Kuvychko, I. V.; Shustova, N. B.; Chen, Y.-S.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H.

      Chem. Eur. J. 2013, 19, 5070–5080.

  1. 44.Structure of 7,9,12,15,18,20,39,24,45,57-C60(CF3)10(1,2:3,4-O2). The First Regiospecific Diepoxidation of a Fullerene Derivative

      Whitaker, J. B.; Shustova, N. B.; Strauss, S. H; Boltalina, O. V. 

      Acta Chim. Slov. 2013, 60, 577–582 (a special issue in honor of Prof. Žemva).

  1. 43.Phenyl Ring Dynamics in a Tetraphenylethylene-Bridged Metal-Organic Framework: Implications for the Mechanism of Aggregation-Induced Emission

      Shustova, N. B.; Ong, T.-C.; Cozzolino, A. F.; Michaelis, V. K.; Griffin, R. G.; Dincă, M.

      J. Am. Chem. Soc. 2012, 134, 15061–15070.

  1. 42.Conformational Locking by Design: Relating Strain Energy with Luminescence and Stability in Rigid Metal–Organic Frameworks

      Shustova, N. B.; Cozzolino, A. F.; Dincă, M.

      J. Am. Chem. Soc. 2012, 134, 19596–19599.

  1. 41.Turn-On Fluorescence in Tetraphenylethylene-Based Metal-Organic Frameworks: an Alternative to Aggregation-Induced Emission

      Shustova, N. B.; McCarthy, B. D.; Dincă M.    

     J. Am. Chem. Soc. 2011, 133, 20126–20129.

  1. 40.Poly(perfluoroalkylation) of Metallic Nitride Fullerenes Reveals Addition-Pattern Guidelines: Synthesis and Characterization of a Family of Sc3N@C80(CF3)n (n = 2−16) and Their Radical Anions

      Shustova, N. B.; Peryshkov, D. V.; Kuvychko, I. V.; Chen, Y.-S.; Mackey, M. A.; Coumbe, C. E.; Heaps, D. T.; Confait, B. S.; Heine, T.;  

       Phillips, J. P.; Stevenson, S.; Dunsch, L.; Popov, A. A.; Strauss, S. H.; Boltalina, O. V.

       J. Am. Chem. Soc. 2011, 133, 2672–2690.

  1. 39.Nitrogen Directs Multiple Radical Additions to 9,9'-Bi-1-aza(C60-Ih)[5,6]fullerene. X-ray Structure of 6,9,12,15,18-C59N(CF3)5

      Shustova, N. B.; Kuvychko, I. V.; Popov, A. A.; Delius, M.; Dunsch, L.; Anderson, O. P.; Hirsch, A.; Strauss, S. H.; Boltalina, O. V.

      Angew. Chem. Int. Ed. 2011, 50, 5537–5540.

  1. 38.Chemical Tailoring of Fullerene Acceptors: Synthesis, Structures and Electrochemical Properties of Perfluoroisopropylfullerenes

      Shustova, N. B.; Kuvychko, I. V.; Peryshkov, D. V.; Whitaker, J. B.; Larson, B. W.; Chen, Y.-S.; Dunsch, L.; Seppelt, K.; Popov, A. A.;

      Strauss, S. H.; Boltalina, O. V.

      Chem. Commun. 2011, 47, 875–877.

  1. 37.Substituent Effects in a Series of 1,7-C60(R-F)2 Compounds (R-F = CF3, C2F5, n-C3F7, i-C3F7, n-C4F9, s-C4F9, n-C8F17): Electron     affinities, Reduction Potentials and E(LUMO) Values Are Not Always Correlated

      Kuvychko, I. V.; Whitaker, J. B.; Larson, B. W.; Folsom, T. C.; Shustova, N. B.; Avdoshenko, S. M.; Chen, Y.-S.; Wen, H.; Wang, X.

      B.; Dunsch, L.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H.

      Chem. Sci. 2012, 3, 1399–1407.

  1. 36.In Search of Fullerene-Based Superacids: Synthesis, X-ray Structure, and DFT study of C60(C2F5)H

      Kuvychko, I. V.; Shustova, N. B.; Avdoshenko, S. M.; Popov, A. A.; Strauss, S. H.; Boltalina, O. V. 

      Chem. Eur. J., 2011, 17, 8799–8802.

  1. 35.Saturnene Revealed : X-ray Crystal Structure of D5d-C60F20 Formed in Reactions of C60 with AxMFy Fluorinating Agents (A = Alkali Metal; M = 3d Metal)

      Shustova, N. B.; Mazej, Z.; Chen, Y.-S.; Popov, A. A.; Strauss, S. H.; Boltalina, O. V. 

      Angew. Chem. Int. Ed. 2010, 49, 812–815.


  1. 34.High-Temperature and Photochemical Syntheses of C60 and C70 Fullerene Derivatives with Linear Perfluoroalkyl Chains

      Shustova, N. B.; Kareev, I. E.; Kuvychko, I. V.; Whitaker, J. B.; Lebedkin, S. F.; Popov, A. A.; Dunsch, L.; Chen, Y.-S.; Seppelt, K.; Strauss, S.

      H.; Boltalina O. V.

      J. Fluorine Chem. 2010, 131, 1198–1212.

  1. 33.Soluble Chlorofullerenes C60Cl2,4,6,8,10. Synthesis, Purification, Compositional Analysis, Stability, and Experimental/Theoretical Structure Elucidation, Including the X-ray Structure of C1-C60Cl10

      Kuvychko, I. V.; Streletskii, A. V.; Shustova, N. B.; Seppelt, K.; Drewello, Popov, A. A.; Strauss, S. H.; Boltalina, O. V.

      J. Am. Chem. Soc. 2010, 132, 6443–6462.

  1. 32.Redox-Tuning Endohedral Fullerene Spin States: From the Dication to the Trianion Radical of Sc3N@C80(CF3)2 in Five Reversible Single-Electron Steps

      Popov, A. A.; Shustova, N. B.; Svitova, A. L.; Mackey, M. A.; Coumbe, C. E.; Phillips, J. P.; Stevenson, S.; Strauss, S. H.; Boltalina, O. V.;

      Dunsch, L

     Chem.-Eur. J. 2010, 16, 4721–4724.

  1. 31.Unraveling the Electron Spin Resonance Pattern of Nonsymmetric Radicals with 30 Fluorine Atoms: Electron Spin Resonance and Vis-Near-Infrared Spectroelectrochemistry of the Anion Radicals and Dianions of C60(CF3)2n (2n = 2–10) Derivatives and Density Functional Theory-Assisted Assignment

      Popov, A. A.; Kareev, I. E.; Shustova, N. B.; Strauss, S. H.; Boltalina, O. V.; Dunsch, L.

      J. Am. Chem. Soc. 2010, 132, 1709–11721.

  1. 30.Sc3N@(C80-Ih(7))(CF3)14 and Sc3N@(C80-Ih(7))(CF3)16. Endohedral Metallofullerene Derivatives with Exohedral Addends on Four and Eight Triple-Hexagon Junctions. Does the Sc3N Cluster Control the Addition Pattern or Vice Versa?

      Shustova, N. B.; Chen, Y.-S.; Mackey, M. A.; Coumbe C. E.; Phillips, J. P.; Stevenson, S.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H.

      J. Am. Chem. Soc. 2009, 131, 17630–17637.

  1. 29.C1-(C84-C2(11))(CF3)12: Trifluoromethylation Yields Structural Proof of a Minor C84 Cage and Reveals a Principle of Higher Fullerene Reactivity

      Kareev, I. E.; Kuvychko, I. V.; Shustova, N. B., Lebedkin, S. F.; Bubnov, V. P.; Anderson, O. P.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H. 

      Angew. Chem. Int. Ed. 2008, 120, 6204–6207.

  1. 28.Synthesis and X-ray or NMR/DFT Structure Elucidation of Twenty-One New Trifluoromethyl Derivatives of Soluble Cage Isomers of C76, C78, C84, and C90

      Kareev, I. E.; Popov, A. A.; Kuvychko, I. V.; Shustova, N. B., Lebedkin, S. F.; Bubnov, V. P.; Anderson, O. P.; Seppelt, K.; Strauss, S. H.;

      Boltalina, O. V.

      J. Am. Chem. Soc. 2008, 130, 13471–13489.

  1. 27.Molecular and Crystal Structure of the C60F18 Adducts with Bromine and Carbon Disulfide

      Shustova, N. B.; Serov, M.; Troyanov, S. I.

      Fullerenes Nanotubes Carbon Nanostruct. 2008, 16, 597–602.

  1. 26.1,7,16,30,36,47-Hexakis(perfluoroisopropyl)-1,7,16,30,36,47-hexahydro(C60–Ih)[5,6]fullerene

      Shustova, N. B.; Kuvychko, I. V.; Boltalina, O. V.; Strauss, S. H.

      Acta Cryst. 2007, E63, o4575.

  1. 25.ESR-Vis-NIR Spectroelectrochemical Study of C70(CF3)2−· and C70(C2F5)2−· Radical Anions

      Popov, A. A.; Shustova, N. B.; Boltalina, O. V.; Strauss, S. H.; Dunsch, L.

      ChemPhysChem 2008, 9, 431–438.

  1. 24.Synthesis, Spectroscopic and Electrochemical Characterization, and DFT Study of Seventeen C70(CF3)n Derivatives (n = 2, 4, 6, 8, 10, 12)

     Popov, A. A.; Kareev, I. E.; Shustova, N. B.; Lebedkin, S. F.; Strauss, S. H.; Boltalina, O. V.; Dunsch, L.

      Chem. Eur. J. 2008, 14, 107–121.

  1. 23.1,3,7,10,14,17,21,28,31,42,52,55-Dodecakis(trifluoromethyl)-1,3,7,10,14,17,21,28,31,42,52,55-dodecahydro(C60-Ih)[5,6]fullerene Shustova, N. B.; Anderson, O. P.; Boltalina, O. V.; Strauss, S. H.

      Acta Cryst. 2007, E64, o159.

  1. 22.Radical Trifluoromethylation of Sc3N@C80

      Shustova, N. B.; Popov, A. A.; Mackay, M. A.; Coumbe, C. E.; Phillips, J. P.; Stevenson, S.; Strauss, S. H.; Boltalina, O. V.

      J. Am. Chem. Soc. 2007, 129, 11676–11677.

  1. 21.Trifluoromethyl Derivatives of Insoluble Small-HOMO-LUMO-Gap Hollow Higher Fullerenes. NMR and DFT Structure Elucidation of C2-(C74-D3h)(CF3)12, Cs-(C76-Td)(CF3)12, C2-(C78-D3h(5))(CF3)12, Cs-(C80-C2v(5))(CF3)12, and C2-(C82-C2(5))(CF3)12

      Shustova, N. B.; Kuvychko, I. V.; Bolskar, R. D.; Seppelt, K.; Strauss, S. H.; Boltalina, O. V.

      J. Am. Chem. Soc. 2006, 128, 15793–15798.

  1. 20.Discovering and Verifying Fullerene Cage Isomers: Structures of C2-p11-(C74-D3h)(CF3)12 and C2-p11-(C78-D3h(5))(CF3)12

         Shustova, N. B.; Newell, B. S.; Miller, S. M.; Anderson, O. P.; Bolskar, R. D.; Seppelt, K.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H.

      Angew. Chem. Int. Ed. 2007, 46, 4111–4114.

  1. 19. Electrochemical, Spectroscopic, and DFT Study of C60(CF3)n Frontier Orbitals (n = 2–18): The Link between Double Bonds

      in Pentagons and Reduction Potentials

      Popov, A. A.; Kareev, I. E.; Shustova, N. B.; Stukalin, E. B.; Lebedkin, S. F.; Seppelt, K.; Strauss, S. H.; Boltalina, O. V.; Dunsch, L.

      J. Am. Chem. Soc. 2007, 129, 11551–11568.

  1. 18.Thermally-Stable Perfluoroalkylfullerenes With the Skew-Pentagonal Pyramid Pattern: C60(C2F5)4O, C60(CF3)4O, and C60(CF3)6

     Kareev, I. E.; Shustova, N. B.; Kuvychko, I. V.; Lebedkin, S. F.; Miller, S. M.; Anderson, O. P.; Popov, A. A.; Strauss, S. H.; Boltalina, O. V.

       J. Am. Chem. Soc. 2006, 128, 12268–12280.

  1. 17.1,6,11,18,24,27,33,51,54,60-Decakis(trifluoromethyl)-1,6,11,18,24,27,33,51,54,60-decahydro(C60-Ih)[5,6]fullerene

      Shustova, N. B.; Peryshkov, D. V.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H.    

      Acta Cryst. 2007, E63, o3129.

  1. 16.1,6,11,18,24,27,33,51,54,60-Octakis(trifluoromethyl)-1,6,11,18,24,27,33,-51,54,60-octahydro(C60-Ih)[5,6]fullerene Deuterochloroform Solvate

      Shustova, N. B.; Peryshkov, D. V.; Kareev, I. E.; Boltalina, O. V.; Strauss, S. H.

      Acta Cryst. 2007, E63, o3398.

  1. 15.1,4,7,11,18,21,24,31,35,39,51,58,61,64-Tetradecakis(trifluoromethyl)-1,4,7,11,18,21,24,-31,35,39,51,58,61,64-tetradecahydro(C70–D5h)[5,6]fullerene p-xylene Trisolvate

      Shustova, N. B.; Peryshkov, D. V.; Kareev, I. E.; Boltalina, O. V.; Strauss, S. H.

      Acta Cryst. 2007, E63, o3928–o3929.

  1. 14.X-ray Structure and DFT Study of C1-C60(CF3)12. A High-Energy Kinetically-Stable Isomer Prepared at 500 °C

      Kareev, I. E.; Shustova, N. B.; Peryshkov, D. V.; Lebedkin, S. F.; Miller, S. M.; Anderson, O. P.; Popov, A. A.; Boltalina, O. V.; Strauss, S. H.

      Chem. Commun. 2007, 1650–1652.

  1. 13.1,4,10,19,25,41,55,60,67,69-Decakis(trifluoromethyl)-1,4,10,19,25,41,55,60,67,69-decahydro(C70-D5h)[5,6]fullerene

      Shustova, N. B.; Peryshkov, D. V.; Boltalina, O. V.; Strauss, S. H.

      Acta Cryst. 2007, E63, o4073.

  1. 12.1,6,11,18,24,27,52,55-Octakis(trifluoromethyl)-1,6,11,18,24,27,52,55-octahydro(C60-Ih)[5,6]fullerene

       Kareev, I. E.; Shustova, N. B.; Newell, B. S.; Miller, S. M.; Anderson, O. P.; Strauss, S. H.; Boltalina, O. V.

       Acta Cryst. 2006, E62, o3154–o3156.

  1. 11.Structure of Halofullerenes Using Experimental and Theoretical Approaches

      Troyanov, S.; Shustova, N.; Popov, A.; Ioffe, I.; Kemnitz, E.

      Acta Cryst. 2005, A61, 19–20.

  1. 10.Crystal Structure C60 Prepared by a Reaction C60 with POCl3

     Shustova, N. B.; Chernyshev, D. Y.; Troyanov S. I.

      Mendeleev Commun. 2006, 4, 209–210.

  1. 9.  Preparation and Structural Characterization of Two Kinetically Stable Chlorofullerenes, C60Cl28 and C60Cl30

      Troyanov, S. I.; Shustova, N. B.; Popov, A. A.; Sidorov, L. N.; Kemnitz, E.

      Angew. Chem. Int. Ed. 2005, 44, 432–435.

  1. 8.  Preparation and Crystallographic Characterization of C60Cl24

      Shustova, N. B.; Popov, A. A.; Sidorov, L. N.; Turnbull, A. P.; Kemnitz, E.; Troyanov, S. I.

      Chem. Commun. 2005, 1411–1413.

  1. 7. Synthesis and Structure of the Highly Chlorinated [60]fullerene C60Cl30 with a Drum-Shaped Carbon Cage

      Troshin, P. A.; Lyubovskaya, R. N., Ioffe, I. N.; Shustova, N. B.; Kemnitz, E.; Troyanov, S. I.

      Angew. Chem. Int. Ed. 2005, 44, 234–237.

  1. 6.  Synthesis and Structural Characterization of Highly Chlorinated C70, C70Cl28

         Troyanov, S. I.; Shustova, N. B.; Ioffe, I. N.; Turnbull, A. P.; Kemnitz, E.       

         Chem. Commun. 2005, 72–74.

  1. 5.  Synthesis and Structure of C60 Fullerene Chlorides

      Troyanov, S. I.; Shustova, N. B.; Popov, A. A.; Sidorov, L.N.

      Russ. Chem. Bull. 2005, 54, 1656–1666.

  1. 4.  Electron Affinity and Suppression Effect in Analysis of Chlorofullerenes by MALDI Mass Spectrometry

      Sidorov, L. N.; Livadaris, V.; Shustova, N. B.; Ioffe, I. N.; Kemnitz, E.; Тroyanov, S. I.

      Russ. Chem. Bull. 2005, 54, 1121–1124.

  1. 3.  Synthesis and Properties of Inorganic Compounds Fullerene C60 and C70 Chlorination using Chlorides SbCl5 and VCl4

      Troyanov, S. I.; Shustova, N. B., Popov, A. A.; Feist, M.; Kemnitz, E.

      Russ. J. Inorg. Chem. 2004, 49, 1303–1307.

  1. 2.   Neganive Ions of Trifluoromethyl Fullerene Derivatives: First Thermodynamic Data

      Alyoshina V. E., Borshchevsky A. Ya., Dorozhkin E. I., Goryunkov A. A., Astakhov A. V., Shustova N. B., Ovchinnikova N. S.

      Fullerenes, Nanotubes, and Carbon Nanostruct. 2003, 12, 201–207.

  1. 1.  Fluorination of the Cubic and Hexagonal C60 Modifications by Crystalline Manganese Trifluoride

      Aleshina, V. E.; Borschevskii, A. Ya.; Skokan, E. V.; Arhangelskii, I. V.; Astahov, A. V.; Shustova, N. B. 

      Phys. Solid State 2002, 44, 629–630.


































© 2013 The Shustova Research Group
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49. Energy Transfer on Demand: Photoswitch-Directed Behavior of Metal−Porphyrin Frameworks

      Williams, D. E.; Rietman, J. A.; Maier, J. M.; Tan, R.; Greytak, A. B.; Smith, M. D.; Krause, J. A.; Shustova, N. B.

       J. Am. Chem. Soc. 2014, 136, 11886–11889.

  1. 54.A Mimic of the Green Fluorescent Protein β-barrel: Photophysics and Dynamics of Confined Chromophores Defined by a Rigid Porous Scaffold

      Williams, D. E.; Dolgopolova, E. A.; Pellechia, P.J.; Palukoshka, A.; Wilson, T. J.; Tan, R.; Maier, J. M.; Tan, R.; Greytak, A. B.; Smith, M. D.; 

      Krause, J. A.;  Shustova, N. B.

      J. Am. Chem. Soc. 2015, 137, 22232226.

     Highlighted in “Noteworthy Chemistry”

    Highlighted in “Nanoreactors: Small Spaces, Big Implications in Chemistry”

53. A Bio-inspired Approach for Chromophore Communication: Ligand-to-Ligand and Host-to-Guest Energy Transfer in Hybrid

  1. Crystalline Scaffolds

      Dolgopolova, E. A.; Williams, D. E.; Greytak, A. B.; Rice, A. M.; Smith, M. D.; Krause, J. A.; Shustova, N. B.

       Angew. Chem. Int. Ed. 2015, 54, 13639–13643.

52. Metal-Organic Frameworks as a Versatile Tool To Study and Model Energy Transfer Processes

      Williams, D. E.; Shustova, N. B.

       Chem. Eur. J. 2015, 21, 15474–15479.

  1. 51.Active Sites in Copper-based Metal-Organic Frameworks: Understanding Substrate Dynamics, Redox Processes, and Valence-Band Structure

      Duke, A. S.; Dolgopolova, E. A.; Galhenage, R. P.; Ammal, S. C.; Heyden, A.; Smith, M. D.; Chen, D. A.; Shustova, N. B.

      J. Phys. Chem. C, 2015, 119, 27457–27466.

  1. 50.Supramolecular Assembly of Metal-Organic Tubes Constructed from the Ditopic Heteroscorpionate Ligand (4-NH2C6H4)CHpz2 (pz = Pyrazol-1-yl) and Silver(I) ransfer Processes

      Gardinier, J. R.; Hewage, J. S.; Hoffman, J. H; Lindeman, S. V.; Williams, D. E.; Shustova, N. B.

       Chem. Eur. J. 2016, 2615–2625

55. Redox-Active Corannulene Buckybowls in a Crystalline Hybrid Scaffold

      Fellows, B. W.; Rice, A. M; Williams, D. E.; Dolgopolova, E. A.; Vannucci, A. K.; Pellechia, P.J.; Smith, M. D.; Krause, J. A.;  Shustova, N. B.

      Angew. Chem. Int. Ed. 2016, 55, 2195–2199.

      Article featured on the cover of the Angew. Chem. Int. Ed.

56. Photophysics of GFP-related Chromophores Imposed by a Scaffold Design

      Dolgopolova, E. A.; Moore, T. M.; Fellows, W. B.; Smith, M. D.; Shustova, N. B.

      Dalton Trans. (New Talents: Americas), 2016, 45, 9884–9881.   

58. Photophysics, Dynamics, and Energy Transfer in Rigid Mimics of GFP-based Systems

      Dolgopolova, E. A.; Rice, A. M.; Smith, M. D.; Shustova, N. B.

      Inorg. Chem. 2016, 55, 7257–7264.

    

57. Fulleretic Well-Defined Scaffolds: Donor-Fullerene Alignment Through Metal Coordination and Its Effect on Photophysics

      Williams, D. E.; Dolgopolova, E. A.; Godfrey, D. C.; Ermolaeva, E. D. Pellechia, P. J.; Greytak, A. B.; Smith, M. D.; Avdoshenko, S. M; Popov, A. A.; Shustova, N. B.

      Angew. Chem. Int. Ed. 2016, 55, 9070–9074.

     

59. Metal-Organic Framework Photophysics: Optoelectronic Devices, Photoswitches, Sensors, and Photocatalysts

      Dolgopolova, E. A.; Shustova, N. B.

      MRS Bull. 2016, 41, 890–896.

      Ekaterina’s artwork is featured on the cover of the MRS Bull.


    

61. Hierarchical Corannulene-Based Materials: Energy Transfer, and Solid-State Photophysics

      Rice, A. M.; Fellows, B. W.; Dolgopolova, E. A.; Greytak, A. B.; Vannucci, A. K.; Smith, M. D.; Karakalos S. G.; Krause, J. A.; Avdoshenko, S. M;

      Popov, A. A.; Shustova, N. B.

      Angew. Chem. Int. Ed. 2017, 56, 4525–4529.


    

  1. 62.Electronic Properties of Bimettalic Metal-Organic Frameworks (MOFs): Tailoring the Density of Electronic States Through MOF  Modularity

      Dolgopolova, E. A.;  Brandt, A. J.; Ejegbavwo, O. A.; Duke, A. S.; Maddumapatabandi, T. D.; Galhenage, R. P.; Larson, B. W.; Reid, O. G.; Ammal, S. A. ;

      Heyden, A.;  Chandrashekhar, Mvs.; Stavila, V.; Chen, D. A.; Shustova, N. B.

      J. Am. Chem. Soc. 2017, 139, 5201–5209.

    

60. A Metal-Organic Framework as a Flask: Photophysics of Confined Chromophores with a Benzylidene Imidazolinone Core

      Dolgopolova, E. A.; Moore, T.; Ejegbavwo, O. A.; Pellechia P. J.;  Shustova, N. B.

      Chem. Commun. (Emerging Investigator Issue) 2017, DOI: 10.1039/C7CC02253K