Beyond Chiral Organic (p-Block) Chromophores for Circularly Polarized Luminescence: The Success of d-Block and f-Block Chiral Complexes

被引:99
作者
Doistau, Benjamin [1 ]
Jimenez, Juan-Ramon [1 ]
Piguet, Claude [1 ]
机构
[1] Univ Geneva, Dept Inorgan & Analyt Chem, Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
circularly polarized luminescence (CPL); coordination complexes; lanthanides; chromium(III); dissymmetry factor; CYCLOMETALATED IRIDIUM(III) COMPLEXES; OPTICAL-ACTIVITY; LANTHANIDE COMPLEXES; SUPRAMOLECULAR CHIRALITY; PHOTOPHYSICAL PROPERTIES; LIQUID-CRYSTAL; DIASTEREOSELECTIVE FORMATION; PLATINUM(II) COMPLEXES; COORDINATION-COMPOUNDS; POLYPYRIDYL COMPLEXES;
D O I
10.3389/fchem.2020.00555
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral molecules are essential for the development of advanced technological applications in spintronic and photonic. The best systems should produce large circularly polarized luminescence (CPL) as estimated by their dissymmetry factor (g(lum)), which can reach the maximum values of -2 <= g(lum) <= 2 when either pure right- or left-handed polarized light is emitted after standard excitation. For matching this requirement, theoretical considerations indicate that optical transitions with large magnetic and weak electric transition dipole moments represent the holy grail of CPL. Because of their detrimental strong and allowed electric dipole transitions, popular chiral emissive organic molecules display generally moderate dissymmetry factors (10(-5) <= g(lum) <= 10(-3)). However, recent efforts in this field show thatg(lum)can be significantly enhanced when the chiral organic activators are part of chiral supramolecular assemblies or of liquid crystalline materials. At the other extreme, chiral Eu-III- and Sm-III-based complexes, which possess intra-shell parity-forbidden electric but allowed magnetic dipole transitions, have yielded the largest dissymmetry factor reported so far with g(lum) similar to 1.38. Consequently, 4f-based metal complexes with strong CPL are currently the best candidates for potential technological applications. They however suffer from the need for highly pure samples and from considerable production costs. In this context, chiral earth-abundant and cheap d-block metal complexes benefit from a renewed interest according that their CPL signal can be optimized despite the larger covalency displayed by d-block cations compared with 4f-block analogs. This essay thus aims at providing a minimum overview of the theoretical aspects rationalizing circularly polarized luminescence and their exploitation for the design of chiral emissive metal complexes with strong CPL. Beyond the corroboration that f-f transitions are ideal candidates for generating large dissymmetry factors, a special attention is focused on the recent attempts to use chiral Cr-III-based complexes that reach values of g(lum)up to 0.2. This could pave the way for replacing high-cost rare earths with cheap transition metals for CPL applications.
引用
收藏
页数:27
相关论文
共 237 条
[1]   NMR, relaxometric, and structural studies of the hydration and exchange dynamics of cationic lanthanide complexes of macrocyclic tetraamide ligands [J].
Aime, S ;
Barge, A ;
Bruce, JI ;
Botta, M ;
Howard, JAK ;
Moloney, JM ;
Parker, D ;
de Sousa, AS ;
Woods, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (24) :5762-5771
[2]   Light-induced control of textures and cholesteric pitch in liquid crystals containing chromium complexes, by means of circular and linear polarized light [J].
Anzai, N ;
Machidat, S ;
Horie, K .
LIQUID CRYSTALS, 2003, 30 (03) :359-366
[3]  
Anzai N, 2001, CHEM LETT, P888
[4]   Light-induced formation of curved needle texture by circularly polarized light irradiation on a discotic liquid crystal containing a racemic chromium complex [J].
Anzai, Nobuhiro ;
Kurihara, Hiroko ;
Sone, Masato ;
Furukawa, Hidemitsu ;
Watanabe, Toshiyuki ;
Horie, Kazuyuki ;
Kumar, Sandeep .
LIQUID CRYSTALS, 2006, 33 (06) :671-679
[5]   Bis(dipyrrinato)zinc(II) Complex Chiroptical Wires: Exfoliation into Single Strands and Intensification of Circularly Polarized Luminescence [J].
Aoki, Risa ;
Toyoda, Ryojun ;
Koegel, Julius F. ;
Sakamoto, Ryota ;
Kumar, Jatish ;
Kitagawa, Yasutaka ;
Harano, Koji ;
Kawai, Tsuyoshi ;
Nishihara, Hiroshi .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (45) :16024-16027
[6]   Syntheses and photophysical properties of optical-active blue-phosphorescent iridium complexes bearing asymmetric tridentate ligands [J].
Ashizawa, Misa ;
Yang, Lifen ;
Kobayashi, Katsuaki ;
Sato, Hisako ;
Yamagishi, Akihiko ;
Okuda, Fumio ;
Harada, Takunori ;
Kuroda, Reiko ;
Haga, Masa-aki .
DALTON TRANSACTIONS, 2009, (10) :1700-1702
[7]   Chiral lanthanide complexes: Coordination chemistry and applications [J].
Aspinall, HC .
CHEMICAL REVIEWS, 2002, 102 (06) :1807-1850
[8]   Chromium(III) Bis-Arylterpyridyl Complexes with Enhanced Visible Absorption via Incorporation of Intraligand Charge-Transfer Transitions [J].
Barbour, Johanna C. ;
Kim, Amy J. I. ;
deVries, Elsemarie ;
Shaner, Sarah E. ;
Lovaasen, Benjamin M. .
INORGANIC CHEMISTRY, 2017, 56 (14) :8212-8222
[9]   Chirality and life [J].
Barron, Laurence D. .
SPACE SCIENCE REVIEWS, 2008, 135 (1-4) :187-201
[10]   Porphyrin sensitization of circularly polarised near-IR lanthanide luminescence: enhanced emission with nucleic acid binding [J].
Beeby, A ;
Dickins, RS ;
FitzGerald, S ;
Govenlock, LJ ;
Maupin, CL ;
Parker, D ;
Riehl, JP ;
Siligardi, G ;
Williams, JAG .
CHEMICAL COMMUNICATIONS, 2000, (13) :1183-1184