2024
107. Lee, T.;¶ Jang, J.-H.;¶ Nguyen, N. N. T.; Jung, J.;* Lee, J.-H.;* Lee, M. H.*, “Ortho-Carborane Decorated Multi-Resonance TADF Emitters: Preserving Local Excited State and High Efficiency in OLEDs”, Adv. Sci., 2024, 11, 2309016.
2023
106. Lee, Y. H.;¶ Ji, J.;¶ Tran, T. Q.; Lee, T.; Jung, J.; Lee, Y.;* Yoo, S.;* Lee, M. H.*, “TADF emitters based on tri-spiral acridine donor and spiro-B-heterotriangulene acceptor: toward high horizontal dipole orientation and high-efficiency deep-blue OLEDs”, Mater. Chem. Front., 2023, 7, 5413-5421.
105. Mubarok, H.;¶ Amin, Al.;¶ Lee, T.; Jung, J.;* Lee, J.-H.;* Lee, M. H.*, “Triptycene-Fused Sterically Shielded Multi-Resonance TADF Emitter Enables High-Efficiency Deep Blue OLEDs with Reduced Dexter Energy Transfer”, Angew. Chem. Int. Ed., 2023, 62, e202306879.
104. Rajakannu, P.;¶ Lee, W.;¶ Park, S.; Kim, H. S.; Mubarok, H.; Lee, M. H.*; *Yoo, S.*, “Molecular Engineering for Shortening the Pt···Pt Distances in Pt(II) Dinuclear Complexes and Enhancing the Efficiencies of these Complexes for Application in Deep-Red and Near-IR OLEDs”, Adv. Funct. Mater., 2023, 33, 2211853.
103. Istiqomah, I. N.;¶ Jang, J.-H.;¶ Lee, T.;¶ Lee, Y. H.; Kim, C.; Jung, J.;* Lee, J.-H.;* Lee, M. H.*, “Impact of p-Expanded Boron-Carbonyl Hybrid Acceptors on TADF Properties: Controlling Local Triplet Excited States and Unusual Emission Tuning”, ACS Appl. Mater. Interfaces, 2023, 15, 15758-15767.
102. Shin, K.; Lee, E.; Lee, T.; Lee, Y. H.; Kim, D. H.; Kim, C.; Jung, J.;* Jung, B. J.;* Lee, M. H.*, “Efficient TADF from carbon-carbon bonded donor-acceptor molecules based on boron-carbonyl hybrid acceptor”, Dyes Pigm., 2023, 209, 110937.
101. Lee, Y. H.;¶ Lee, W.;¶ Lee, T.; Jung, J.;* Yoo, S.;* Lee, M. H.*, “Achieving over 36% EQE in blue OLEDs using rigid TADF emitters based on spiro-donor and spiro-B-heterotriangulene acceptors”, Chem. Eng. J., 2023, 452, 139387.
2022
100. Singh, N.; Noh, G. H.; Mubarok, H.; Kim, C. W.; Lee, M. H.;* Lee, J.* “Synthesis and photophysical studies on cyclometalated iridium complexes containing various monodentate phenyl-azole ancillary ligands”, Polyhedron, 2022, 227, 116096.
99. Nguyen, N. N. T.;¶ Mubarok, H.;¶ Lee, T.; Tran, T. Q.; Jung, J.;* Lee, M. H.*, “Highly emissive planarized B,N-diarylated benzonaphthoazaborine compounds for narrowband blue fluorescence” ”, RSC Adv., 2022, 12, 29892-29899.
98. Kwak, S. W.;† Mubarok, H.;† Lee, J. H.; Hwang, H.; Lee, K. M.; Lee, M. H.;* Park, M. H.*, “Highly red-emissive salen–indium complexes: impact of 4-amino-substitution on the photophysical properties”, Inorg. Chem. Front., 2022, 9, 119-126.
2021
97. Lee, Y. H.;¶ Shin, Y.-S;¶ Lee, T.; Jung, J.;* Lee, J.-H.;* Lee, M. H.*, “Managing local triplet excited states of boron-based TADF emitters for fast spin-flip process: Toward highly efficient TADF-OLEDs with low efficiency roll-off”, Chem. Eng. J., 2021, 423, 130224.
96. Lee, Y. H.;¶ Lee, W.;¶ Lee, T.; Lee, D.; Jung, J.;* Yoo, S.;* Lee, M. H.*, “Blue TADF Emitters Based on B-Heterotriangulene Acceptors for Highly Efficient OLEDs with Reduced Efficiency Roll-Off”, ACS Appl. Mater. Interfaces, 2021, 13, 45778-45788.
95. Lee, Y. H.;¶ Lee, D.;¶ Lee, T.; Lee, J.; Jung, J.; Yoo, S.;* Lee, M. H.*, “Impact of boryl acceptors in para-acridine-appended triarylboron emitters on blue thermally activated delayed fluorescence OLEDs”, Dyes Pigm., 2021, 188, 109224.
2020
94. Nguyen, V.-N.; Kumar, A.; Lee, M. H.;* Yoon, J.*, “Recent advances in biomedical applications of organic fluorescence materials with reduced singlet-triplet energy gaps”, Coord. Chem. Rev., 2020, 425, 213545.
93. Kumar, A.; Shin, H. Y.; Lee, T.; Jung, J.;* Jung, B. J.;* Lee, M. H.*, “Doubly Boron-doped TADF Emitters Decorated with ortho-Donor Groups for Highly Efficient Green to Red OLEDs”, Chem. Eur. J., 2020,26, 16793-16801.
92. Lee, Y. H.; Nam, E. B.; Lee, J.; Lee, S. U.;* Lee, M. H.*, “Frustrated Lewis pairs with thermally activated delayed fluorescence properties: activation of formaldehyde”, Dalton Trans., 2020, 49, 13198-13201.
91. Sujith, S.; Nam, E. B.; Lee, J.; Lee, S. U.;* Lee, M. H.*, “Enhancing the thermally activated delayed fluorescence of nido-carborane-appended triarylboranes by steric modification of the phenylene linker”, Inorg. Chem. Front., 2020, 7, 3456-3464.
90. Rajakannu, P.;¶ Kim, H. S.;¶ Lee, W.; Kumar, A.; Lee, M. H.;* Yoo, S.*, “Naphthalene Benzimidazole Based Neutral Ir(III) Emitters for Deep Red Organic Light-Emitting Diodes”, Inorg. Chem., 2020, 59, 12461-12470.
89. Mubarok, H.;¶ Lee, W.;¶ Lee, T.; Jung, J.; Yoo, S.;* Lee, M. H.*, “Impact of Boron Acceptors on the TADF Properties of Ortho-Donor-Appended Triarylboron Emitters”, Front. Chem., 2020, 8, 538.
88. Kim, J.; Lee, T.; Ryu, J. Y.; Lee, Y. H.; Lee, J.; Jung, J.;* Lee, M. H.*, “Highly Emissive ortho-Donor–Acceptor Triarylboranes: Impact of Boryl Acceptors on Luminescence Properties”, Organometallics, 2020,39, 2235-2244.
87. Kumar, A.;† Lee, W.;† Lee, T.; Jung, J.;* Yoo, S.;* Lee, M. H.*, “Triarylboron-based TADF emitters with perfluoro substituents: high-efficiency OLEDs with a power efficiency over 100 lmW−1”, J. Mater. Chem. C, 2020, 8, 4253-4263.
86. Lee, H.; Jana, S.; Kim, J.; Lee, S. U.;* Lee, M. H.*, “Donor–Acceptor-Appended Triarylboron Lewis Acids: Ratiometric or Time-Resolved Turn-On Fluorescence Response toward Fluoride Binding”, Inorg. Chem., 2020, 59, 1414-1423.
2019
85. Kumar, A.; Oh, J.; Kim, J.; Jung, J.;* Lee, M. H.*, “Facile color tuning of thermally activated delayed fluorescence by substituted ortho-carbazole-appended triarylboron emitters”, Dyes Pigm., 2019, 168, 273-280.
2018
84. Nghia, N. V.; Oh, J.; Sujith, S.; Jung, J.;* Lee, M. H.*, “Tuning the photophysical properties of carboranyl luminophores by closo- to nido-carborane conversion and application to OFF-ON fluoride sensing”, Dalton Trans., 2018, 47, 17441-17449.
83. Lee, Y. H.; Jana, S.; Lee, H.; Lee, S. U.;* Lee, M. H.*, “Rational design of time-resolved turn-on fluorescence sensors: exploiting delayed fluorescence for hydrogen peroxide sensing”, Chem. Commun., 2018, 54, 12069-12072.
82. Ryu, J. Y.; Lee, J. M.; Nghia, N. V.; Lee, K. M.; Lee, S.; Lee, M. H.;* Stang, P. J.;* Lee, J.*, “Supramolecular Pt(II) and Ru(II) Trigonal Prismatic Cages Constructed with a Tris(pyridyl)borane Donor”, Inorg. Chem., 2018, 57, 11696-11703.
81. Nghia, N. V.; Jana, S.; Sujith, S.; Ryu, J. Y.; Lee, J.; Lee, S. U.;* Lee, M. H.*, “Nido-Carboranes: Donors for Thermally Activated Delayed Fluorescence”, Angew. Chem. Int. Ed., 2018, 57, 12483-12488.
80. Lee, Y. H; Park, S.; Oh, J; Woo, S.-J.; Kumar, A.; Kim, J.-J.; Jung, J.;* Yoo, S.;* Lee, M. H.*, “High-Efficiency Sky Blue to Ultra-Deep Blue Thermally Activated Delayed Fluorescent Diodes Based on Ortho-Carbazole-Appended Triarylboron Emitters: Above 32% External Quantum Efficiency in Blue Devices”, Adv. Opt. Mater., 2018, 6, 1800385.
79. Kim, M.; Lee, M. H.*, “Deep blue phosphorescent iridium(III) cyclometalates with o-carboranes”, J. Organomet. Chem., 2018, 870, 1-7.
2017
78. Kumar, A; Yang, M.; Kim, M; Gabbaï, F. P.;* Lee, M. H.*, “OFF-ON Fluorescence Sensing of Fluoride by Donor-Antimony(V) Lewis Acids”, Organometallics, 2017, 36, 4901-4907.
77. Lee, Y. H.; Lee, H. D.; Ryu, J. Y.; Lee, J.; Lee, M. H.*, “Photophysical and Lewis acidic properties of triarylboranes with meta-substituted 2-R-o-carboranes”, J. Organomet. Chem., 2017, 846, 81-87.
76. Nghia, N. V; Oh, J.; Jung, J.;* Lee, M. H.*, “Deboronation-Induced Turn-on Phosphorescent Sensing of Fluorides by Iridium(III) Cyclometalates with o-Carborane”, Organometallics, 2017, 36, 2573-2580.
75. Lee, Y. H.; Park, S.; Oh, J.; Shin, J. W.; Jung, J.;* Yoo, S.;* Lee, M. H.*, “Rigidity-Induced Delayed Fluorescence by Ortho Donor-Appended Triarylboron Compounds: Record-High Efficiency in Pure Blue Fluorescent Organic Light-Emitting Diodes”, ACS Appl. Mater. Interfaces, 2017, 9, 24035-24042.
74. You, D. K.; Lee, J. H.; Choi, B. H.; Hwang, H.; Lee, M. H.*; Lee, K. M.*; Park, M. H.*, “Effects of multi-carborane substitution on the photophysical and electron accepting properties of o-carboranylbenzene compounds”, Eur. J. Inorg. Chem., 2017, 2496-2503.
73. Nghia, N. V.; Park, S.; An, Y.; Lee, J.; Jung, J.; Yoo, S.;* Lee, M. H.*, “Impact of the number of o-carboranyl ligands on the photophysical and electroluminescent properties of iridium(III) cyclometalates”, J. Mater. Chem. C, 2017, 5, 3024-3034.
2016
72. Park, J.; Lee, Y. H.; Ryu, J. Y.; Lee, J.; Lee, M. H.*, “The substituent effect of 2-R-o-carborane on the photophysical properties of iridium(III) cyclometalates”, Dalton Trans., 2016, 45, 5667-5675.
71. Kim, Y.; Park, S.; Lee, Y. H.; Jung, J.; Yoo, S;* Lee, M. H.*, “Homoleptic Tris-Cyclometalated Iridium Complexes with Substituted o-Carboranes: Green Phosphorescent Emitters for Highly Efficient Solution- Processed Organic Light-Emitting Diodes”, Inorg. Chem., 2016, 55, 909-917.
2015
70. Kim, T.; Lee, J.; Lee, S. U.;* Lee, M. H.*, “o-Carboranyl-Phosphine as a New Class of Strong-Field Ancillary Ligand in Cyclometalated Iridium(III) Complexes: Toward Blue Phosphorescence”,Organometallics, 2015, 34, 3455-3458.
69. Lee, Y. H.; Park, J.; Lee, J.; Lee, S. U.;* Lee, M. H.*, “Iridium Cyclometalates with Tethered o-Carboranes: Impact of Restricted Rotation of o-Carborane on Phosphorescence Efficiency”, J. Am. Chem. Soc., 2015, 137, 8018.
68. Kim, T.; Lim, S.; Park, S.-R.; Han, C. J.;* Lee, M. H.*, “Polynorbornene Copolymer with Side-Chain Triarylborane and Iridium(III) Groups: An Emissive Layer Material with Electron Transporting Properties for PhOLEDs”, Polymer, 2015, 66, 67-75.
67. Park, Y. J.; Ryu, J. Y.; Begum, H.; Lee, M. H.; Stang, P. J.;* Lee, J.*, “Selective Formation of Heterometallic Ru−Ag Supramolecules via Stoichiometric Control of Multiple Different Tectons”, J. Am. Chem. Soc., 2015, 137, 5863-5866.
66. Kwak, J.; Nghia, N. V.; Lee, J.; Kim, H.;* Park, M. H.;* Lee, M. H.*, “Lewis acidity enhancement of triarylborane by appended phosphine oxide groups”, Dalton Trans., 2015, 44, 4765-4772.
65. Lee, Y. H.; Park, J.; Jo, S.-J.; Kim, M.; Lee, J.;* Lee, S. U.;* Lee, M. H.*, “Manipulation of Phosphorescence Efficiency of Cyclometalated Iridium Complexes by Substituted o-Carboranes”, Chem. Eur. J., 2015, 21, 2052-2061.
64. Sung, W. Y.; Lee, J.; Lee, M. H.*, “Triarylborane Lewis acids with indole or phenol group: B/H hybrid receptors for fluoride”, J. Organomet. Chem., 2015, 776, 143-148.
2014
63. Sharma, S.; Kim, H.; Lee, Y. H.; Kim, T.; Lee, Y. S.; Lee, M. H.*, “Heteroleptic Cyclometalated Iridium(III) Complexes Supported by Triarylborylpicolinate Ligand: Ratiometric Turn-On Phosphorescence Response upon Fluoride Binding”, Inorg. Chem., 2014, 53, 8672-8680.
62. Cho, S.;* Nho, S.-H.; Eo, M.; Lee, M. H.*, “Effects of processing additive on bipolar field-effect transistors based on blends of poly(3-hexylthiophene) and fullerene bearing long alkyl tails”, Org. Electron., 2014, 15, 1002-1011.
61. Bae, H. J.; Kim, H.; Lee, K. M.; Kim, T.; Lee, Y. S.; Do, Y.;* Lee, M. H.*, “Through-space charge transfer and emission color tuning of di-o-carborane substituted benzene”, Dalton Trans., 2014, 43, 4978-4985.
60. Lee, Y. H.; Nghia, N. V.; Go, M. J.; Lee, J.; Lee, S. U.;* Lee, M. H.*, “Terpyridine-Triarylborane Conjugates for the Dual Complexation of Zn(II) Cation and Fluoride Anion”, Organometallics, 2014, 33, 753-762.
59. Eo, M.; Han, D.; Park, M. H.; Hong, M.; Do, Y.;* Yoo, S.;* Lee, M. H.*, “Polynorbornenes with Pendant PCBM as an Acceptor for OPVs: Ring-opening Metathesis versus Vinyl-addition Polymerization”, Eur. Polym. J., 2014, 51, 37-44.
58. Bae, H. J.; Chung, J.; Kim, H.; Park, J.; Lee, K. M.; Koh, T.-W.; Lee, Y. S.; Yoo, S.;* Do, Y.;* Lee, M. H.*, “Deep Red Phosphorescence of Cyclometalated Iridium Complexes by o-Carborane Substitution”,Inorg. Chem., 2014, 53, 128-138.
2013
57. Ryu, J. Y.; Lee, J. M.; Park, Y. J.; Nghia, N. V.; Lee, M. H.*; Lee, J.*, “A Ruthenium Iron Bimetallic Supramolecular Cage with D4 Symmetry from a Tetrapyridyl Iron(I) Metalloligand”, Organometallics, 2013,32, 7272-7274.
56. Eo, M.; Park, M. H.; Kim, T.; Do, Y.;* Lee, M. H.*, “Polynorbornene copolymers with pendent o-carborane and carbazole groups: Novel side-chain donor acceptor copolymers for turn-on sensing of nucleophilic anions”, Polymer, 2013, 54, 6321-6328.
55. Bae, H. J.; Kim, H.; Lee, K. M.; Kim, T.; Eo, M.; Lee, Y. S.; Do, Y.; Lee, M. H.*, “Heteroleptic tris-cyclometalated iridium(III) complexes supported by an o-carboranyl-pyridine ligand”, Dalton Trans., 2013, 42, 8549-8552.
54. Eo, M.; Bae, H. J.; Hong, M.; Do, Y.;* Cho, S.;* Lee, M. H.*, “Synthesis and Electron Transporting Properties of Methanofullerene-o-Carborane Dyads in Organic Field-Effect Transistors”, Dalton Trans., 2013, 42, 8104-8112.
53. Song, K. C; Lee, K. M.; Nghia, N. V.; Sung, W. Y.; Do, Y.;* Lee, M. H.*, “Synthesis and Anion Binding Properties of Multi-phosphonium Triarylboranes: Selective Sensing of Cyanide Ions in Buffered Water at pH 7”, Organometallics, 2013, 32, 817-823.
52. Park, J. H.; Koh, T.-W.; Chung, J.; Park, S. H.; Eo, M.; Do, Y.;* Yoo, S.;* Lee, M. H.*, “Polynorbornene Copolymer with Side-Chain Iridium(III) Emitters and Carbazole Hosts: A Single Emissive Layer Material for Highly Efficient Electrophosphorescent Devices”, Macromolecules, 2013, 46, 674-682.
51. Kim, T.; Kim, H.; Lee, K. M.; Lee, Y. S.;* Lee, M. H.*, “Phosphorescence Color Tuning of Cyclometalated Iridium Complexes by o-Carborane Substitution”, Inorg. Chem., 2013, 52, 160-168.
50. Song, K. C.; Kim, H.; Lee, K. M.; Lee, Y. S.; Do, Y.;* Lee, M. H.*, “Dual Sensing of Fluoride Ions by the o-Carborane-Triarylborane Dyad”, Dalton Trans., 2013, 42, 2351-2354.
49. Song, K. C.; Kim, H.; Lee, K. M.; Lee, Y. S.; Do, Y.;* Lee, M. H.*; “Ratiometric Fluorescence Sensing of Fluoride Ions by Triarylborane Phenanthroimidazole Conjugates”, Sens. Actuators B, 2013, 176, 850-857.
2012
48. Song, K. C.; Lee, K. M.; Kim, H.; Lee, Y. S.; Lee, M. H.*; Do, Y.*, “Turn-On Colorimetric Sensing of Fluoride Ions by a Cationic Triarylborane Bearing Benzothiazolium”, J. Organomet. Chem., 2012, 713, 89-95.
47. Eo, M.; Lee, S.; Park, M. H.; Lee, M. H.*; Yoo, S.;* Do, Y.*, “Vinyl-type Polynorbornenes with Pendant PCBM: A Novel Acceptor for Organic Solar Cells“, Macromol. Rapid Comm., 2012, 33, 1119-1125.
46. Sung, W. Y.; Park, M. H.; Park, J. H.; Eo, M.; Yu, M.-S.; Do, Y.;* Lee, M. H.*, “Triarylborane-Functionalized Polynorbornenes: Direct Polymerization and Signal Amplification in Fluoride Sensing”, Polymer, 2012, 53, 1857-1863.
45. Park, J. H.; Koh, T.-W.; Do, Y.;* Lee, M. H.*; Yoo, S.*, “Soluble Polynorbornenes with Pendant Carbazole Derivatives as Host Materials for Highly Efficient Blue Phosphorescent Organic Light-Emitting Diodes”, J. Polym. Sci., Part A: Polym. Chem., 2012, 50, 2356-2365.
44. Vadavi, R. S.; Kim, H.; Lee, K. M.; Kim, T.; Lee, J.; Lee, Y. S.; Lee, M. H.*, “Turning On MLCT Phosphorescence of Iridium(III) Borane Conjugates upon Fluoride Binding”, Organometallics, 2012, 31, 31-34.
43. Misha, A.; Vajpayee, V.; Kim, H.; Lee, M. H.; Jung, H.; Wang, M.; Stang, P. J.; Chi, K.-W., “Self-assembled Metalla-bowls for Selective Sensing of Multi-carboxylate Anions”, Dalton Trans., 2012, 41, 1095-1201.
42. Lee, M. H.*; Park, M. H.; Sung, W. Y.; Kim S. K.; Son, A.; Do, Y., “A Biphenylene-Bridged Dinuclear Constrained Geometry Titanium Complex for Ethylene and Ethylene/1-Octene Polymerizations”, J. Organomet. Chem., 2012, 696, 4315-4320.
2011
41. Lee, K. M.; Huh, J. O.; Kim, T.; Do, Y.; Lee, M. H.*, “A Highly Lewis Acidic Triarylborane Bearing Peripheral o-Carborane Cages”, Dalton Trans., 2011, 40, 11758-11764.
40. Vajpayee, V.; Song, Y. H.; Lee, M. H.*; Kim, H.; Wang, M.; Stang, P. J.; Chi, K-W., “Self-Assembled Arene-Ruthenium-Based Rectangles for the selective Sensing of Multi-Carboxylate Anions", Chem. Eur. J., 2011, 17, 7837-7844.
39. Park, M. H.; Lee, K. M.; Kim, T.; Do, Y.; Lee, M. H.*, “o-Carborane-Functionalized Luminescent Polyethylene: Potential Chemodosimeter for the Sensing of Nucleophilic Anions”, Chem. Asian J., 2011, 6, 1362-1366. (selected as a Very Important Paper)
38. Park, J. H.; Yun, C.; Koh, T.-W.; Do, Y.; Yoo, S.; Lee, M. H.*, “Vinyl-Type Polynorbornene with 9,9'-(1,1'-Biphenyl)-4,4'-diylbis-9H-
carbazole Side Groups as a Host Material for Highly Efficient Green Phosphorescent Organic Light-Emitting Diodes”, J. Mater. Chem.,
2011, 21, 5422-5429.
37. Vajpayee, V.; Kim H.; Mishra, A.; Mukherjee, P. S.; Stang, P. J.; Lee, M. H.; Kim, H. K.; Chi, K-W., “Self-assembled Molecular Squares Containing Metal-based Donor: Synthesis and Application in the Sensing of Nitro-aromatics”, Dalton Trans., 2011, 40, 3112-3115.
36. Park, M. H.; Kim, T.; Huh, J. O.; Do, Y.; Lee, M. H.*, “Luminescent Polyethylene with Side-Chain Triarylboranes: Synthesis and Fluoride
Sensing Properties”, Polymer, 2011, 52, 1510-1514.
35. Kim, Y.; Huh, H.-S.; Lee, M. H.; Lenov, I. L.; Zhao, H.; Gabbai, F. P., “Turn-On Fluorescence Sensing of Cyanide Ions in Aqueous Solution
at Parts-per-Billion Concentrations”, Chem. Eur. J., 2011, 17, 2057-2062.
- 2010
34. Park, M. H.; Park, J. H.; Do, Y.; Lee, M. H.*, “Metallocene-Catalyzed Synthesis of Polyethylenes with Side-Chain Triarylamines: Effects of Catalyst Structure and Triarylamine Functionality”, Polymer, 2010, 51, 4735-4743.
33. Park, M. H.; Yun, C.; Huh, J. O.; Do, Y.; Yoo, S.; Lee, M. H.*, “Synthesis and Hole-Transporting Properties of Vinyl-Type Polynorbornenes with Ethyl Ester Linked Triarylamine Side Groups”, Synth. Met., 2010, 160, 2000-2007.
32. Shin, C. H.; Huh, J. O.; Baek, S. J.; Kim, S. K.; Lee, M. H.*, Do, Y., “Dinuclear Iridium(III) Complexes Linked by Bis-β-Diketonate Bridging
Ligand: Energy Convergence versus Aggregation-Induced Emission”, Eur. J. Inorg. Chem., 2010, 3642-3651.
31. Huh, J. O.; Kim, H.; Lee, K. M.; Lee, Y. S.; Do, Y.; Lee, M. H.*, “o-Carborane-Assisted Lewis Acidity Enhancement of Triarylboranes”, Chem. Commun., 2010, 46, 1138-1140.
30. Han, Y.; Kim, H.; Lee, M. H.; Kim, Y.; Lee, J.; Lee, Y. S.; Do, Y., “Aminosilylene-Bridged ansa-Zirconocenes for Branched Polyethylenes with Bimodal Molecular Weight Distributions”, J. Organomet. Chem., 2009, 694, 4216-4222.
29. Park, J. H.; Yun, C.; Park, M. H.; Do, Y.; Yoo, S.; Lee, M. H.*, “Vinyl-Type Polynorbornenes with Triarylamine Side Groups: A New Class of Soluble Hole-Transporting Materials for OLEDs”, Macromolecules, 2009, 42, 6840-6843.
28. Shin, C. H.; Huh, J. O.; Lee, M. H.*; Do, Y., “Polymorphism-induced dual phosphorescent emission from solid-state iridium(III) complex”, Dalton Trans., 2009, 6476-6479.
27. Hwang, K. Y.; Kim, H.; Lee, Y. S.; Lee, M. H.*; Do, Y., “Synthesis and Properties of Salen-Aluminum Complexes as a Novel Class of
Color-Tunable Luminophores”, Chem. Eur. J., 2009, 15, 6478-6487.
26. Kim, N. G.; Shin, C. H; Lee, M. H.*; Do, Y., “Four-Coordinate Boron Compounds Derived from 2-(2-Pyridyl)phenol Ligand as Novel
Hole-Blocking Materials for Phosphorescent OLEDs”, J. Organomet. Chem., 2009, 694, 1922-1928.
25. Shin, C. H.; Han, Y.; Lee, M. H.*; Do, Y., “Group 4 ansa-Metallocenes Derived from o-Carborane and Their Luminescent Properties”, J.
Organomet. Chem., 2009, 694, 1623-1631.
24. Kim, H. K.; Kim, S. K.; Park, J. H.; Yoon, S. W.; Lee, M. H.*; Do, Y., “Elaboration of rac-Like Active Species from Lewis Base Functionalized Unbridged Zirconocenes for Isospecific Propylene Polymerization”, Chem. Asian J., 2008, 3, 1912-1921.
23. Huh, J. O.; Lee, M. H.; Jang, H.; Hwang, K. Y.; Lee, J. S.; Kim, S. H.; Do, Y., “A Novel Solution-Processible Heterodinuclear Al(III)/Ir(III) Complex for Host-Dopant Assembly OLEDs”, Inorg. Chem., 2008, 47, 6656-6658.
22. Park, M. H.; Huh, J. O.; Do, Y.; Lee, M. H.*, “Synthesis and Properties of Polyethylene with Side-Chain Triphenylamines as Hole-Transporting Materials”, J. Polym. Sci., Part A: Polym. Chem., 2008, 46, 5816-5825.
21. Huh, J. O.; Do, Y.; Lee, M. H.*, “A BODIPY-Borane Dyad for the Selective Complexation of Cyanide Ion”, Organometallics, 2008, 27, 1022-1025.
20. Hwang, K. Y.; Lee, M. H.; Jang, H.; Sung, Y.; Lee, J. S.; Kim, S. H.; Do, Y., “Aluminum-Salen Luminophores as New Hole-Blocking Materials for Phosphorescent OLEDs”, Dalton Trans., 2008, 1818-1820.
19. Kim, S. K.; Kim, H. K.; Lee, M. H.; Yoon, S. W.; Do, Y., “Novel Synthetic Strategy for Developing an Isospecific Unbridged Metallocene System for Propylene Polymerization”, Chem. Eur. J., 2007, 13, 9107-9114.
18. Lee, M. H.; Gabbai, F. P., “Synthesis and Properties of a Cationic Bidentate Lewis Acid”, Inorg. Chem., 2007, 46, 8132-8138. (Cover Page, Vol. 46, No. 20)
17. Lee, M. H.; Agou, T.; Kobayashi, J.; Kawashima, T.; Gabbai, F. P., “Fluoride Ion Complexation by a Cationic Borane in Aqueous Solution”, Chem. Commun., 2007, 1133-1135.
16. Kim, S. K.; Kim, H. K.; Lee, M. H.; Yoon, S. W.; Han, Y.; Park, S.; Lee, J.; Do, Y., “Dinuclear Metallocenes with a Modulated Biphenylene Bridge for Olefin Polymerization”, Eur. J. Inorg. Chem., 2007, 537-545.
15. Kim, S. K.; Kim, H. K.; Lee, M. H.; Yoon, S. W.; Do, Y., “Endowing Aspecific, Unbridged-Metallocene Propylene-Polymerization Catalysts with Isospecificity: The Unprecedented Role of MAO”, Angew. Chem. Int. Ed., 2006, 45, 6163-6166.
14. Lee, M. H.; Kim, S. K.; Do, Y., “Biphenylene-Bridged Dinuclear Group 4 Metal Complexes: Enhanced Polymerization Properties in Olefin Polymerization”, Organometallics, 2005, 24, 3618-3620.
13. Lee, M. H.; Do, Y., “Zirconocene Complexes with a Biphenyl Substituted Cyclopentadienyl Ligand: Synthesis, Characterization, and Olefin Polymerization Behavior”, J. Organomet. Chem., 2005, 690, 1240-1248.
12. Lee, M. H.; Han, Y.; Kim, D.-h.; Hwang, J.-W.; Do, Y., “Isospecific Propylene Polymerization by C1-Symmetric Me2Si(C5Me4)(2-R-Ind)MCl2 (M = Ti, Zr) Complexes”, Organometallics, 2003, 22, 2790-2796.
11. Han, Y.; Hong, E.; Kim, Y.; Lee, M. H.; Kim, J.; Hwang, J.-W.; Do, Y., "Group 4 Complexes Derived from o-Carborane: Synthesis, Structures, and Ethylene Polymerization Properties", J. Organomet. Chem., 2003, 679, 48-58.
10. Kim, J.; Hwang, J.-W; Kim, Y.; Lee, M. H.; Han, Y.; Do, Y., "Synthesis, Structure, and Ethylene Polymerization Behavior of Zirconium Complexes with Chelating Ketoiminate Ligands.", J. Organomet. Chem., 2001, 620, 1-7.
9. Kim, Y.; Han, Y.; Lee, M. H.; Yoon, S. W.; Choi, K. H.; Song, B. G.; Do, Y., “New Half-Sandwich Metallocene Catalysts Generating Polyethylene with Bimodal Molecular Weight Distribution and Syndiotactic Polystyrene”, Macromol. Rapid Commun., 2001, 22, 573-578.
8. Kim, I.; Kim, K. T.; Lee, M. H.; Do, Y.; Chung, H., " Copolymerization of Ethylene and 1-Decene by Metallocenes: Direct Comparison of
Me2C(Cp)(Flu)ZrMe2 with Et(Cp)(Flu)ZrMe2", Polym. Eng. Sci., 2001, 41, 899-907.
7. Lee, M. H.; Hwang, J.-W.; Kim, Y.; Han, Y.; Do, Y., “Synthesis and Characterization of Group 4 Constrained Geometry Complexes Containing a Linked Cyclopentadienyl-o-Carboranyl Ligand”, Organometallics, 2000, 19, 5514-5517.
6. Lee, M. H.; Hwang, J.-W.; Kim, Y.; Kim, J.; Han, Y.; Do, Y., “The First Fluorenyl ansa-Yttrocene Complexes: Synthesis, Structures, and
Polymerization of Methyl Methacrylate”, Organometallics, 1999, 18, 5124-5129.
5. Kim, Y.; Hong, E.; Lee, M. H.; Kim, J.; Han, Y.; Do, Y., “Pentamethylcyclopentadienyltitanatrane: A New Class of Catalyst for Syndiospecific Polymerization of Styrene”, Organometallics, 1999, 18, 36-39.
4. Kim, I.; Kim, S. Y.; Lee, M. H.; Do, Y.; Won, M.-S., “Ethylene/1-Hexene Copolymerization by Syndioselective Metallocene: Direct Comparison of Me2C(Cp)(Flu)ZrMe2 with Et(Cp)(Flu)ZrMe2”, J. Polym. Sci., Part A: Polym. Chem., 1999, 37, 2763-2772.
3. Kim, I.; Kim, S. Y.; Choi, C.-S.; Lee, M. H.; Do, Y., “Copolymerization of Ethylene and 1-Octene by Syndiospecific Metallocenes: Comparison of Me2C(Cp)(Flu)ZrMe2 with Et(Cp)(Flu)ZrMe2”, Korea Polym. J. (now Macromol. Research), 1999, 7, 162-171.
2. Lee, M. H.; Park, J.-W.; Hong, C. S.; Woo, S. I.; Do, Y., “Ethylene-Bridged pseudo-Cs Symmetric ansa-Zirconocene Complexes: Synthesis,
Structures and Propylene Polymerization Behavior”, J. Organomet. Chem., 1998, 561, 37-47.
1. Kim, I.; Kim, K.-T.; Lee, M. H.; Do, Y.; Won, M.-S., “Syndioselective Propylene Polymerization: Comparison of Me2C(Cp)(Flu)ZrMe2 with Et(Cp)(Flu)ZrMe2”, J. Appl. Polym. Sci., 1998, 70, 973-983.
106. Lee, Y. H.;¶ Ji, J.;¶ Tran, T. Q.; Lee, T.; Jung, J.; Lee, Y.;* Yoo, S.;* Lee, M. H.*, “TADF emitters based on tri-spiral acridine donor and spiro-B-heterotriangulene acceptor: toward high horizontal dipole orientation and high-efficiency deep-blue OLEDs”, Mater. Chem. Front., 2023, 7, 5413-5421.