Recent Highlights in the use of Lanthanide-directed Synthesis of Novel Supramolecular (Luminescent) Self-assembly Structures such as Coordination Bundles, Helicates and Sensors

2011 ◽  
Vol 64 (10) ◽  
pp. 1315 ◽  
Author(s):  
Christophe Lincheneau ◽  
Floriana Stomeo ◽  
Steve Comby ◽  
Thorfinnur Gunnlaugsson

In this short review, we focus on the recent developments within the field of coordination chemistry where mono- or multimetallic supramolecular self-assemblies are formed by employing structurally defined organic ligands, taking advantage of the high coordination requirements of the lanthanides. Such synthesis results in the formation of both structurally complex and beautiful self-assemblies. Moreover, as the lanthanide ions possess both unique magnetic (e.g. GdIII and DyIII) and luminescent properties, either in the visible (EuIII, SmIII and TbIII) or near-infrared regions (YbIII, NdIII, ErIII), these physical features are usually transferred to the self-assemblies themselves, allowing the formation of highly functional structures, such as coordination networks, as well as molecular bundles and helicates. Hence, examples of the use of lanthanide-directed synthesis of luminescent sensors, some of which are formed on solid surfaces such as gold (flat surface or nanoparticles), and imaging agents are presented. Moreover, we demonstrate that by using chiral organic ligands, lanthanide-directed synthesis can also give rise to the formation of enantiomerically pure self-assemblies, the structure of which can be probed using circularly polarized luminescence.

2016 ◽  
Vol 45 (11) ◽  
pp. 3244-3274 ◽  
Author(s):  
Dawn E. Barry ◽  
David F. Caffrey ◽  
Thorfinnur Gunnlaugsson

This review focuses on recent developments made in the area of lanthanide directed synthesis/formation of supramolecular self-assembly structures including the formation of complexes/bundles, helicates, MOFs and interlocked molecules.


2018 ◽  
Vol 90 (9) ◽  
pp. 1393-1407 ◽  
Author(s):  
Leonardo Scarabelli

Abstract The field of plasmonics has grown at an incredible pace in the last couple of decades, and the synthesis and self-assembly of anisotropic plasmonic materials remains highly dynamic. The engineering of nanoparticle optical and electronic properties has resulted in important consequences for several scientific fields, including energy, medicine, biosensing, and electronics. However, the full potential of plasmonics has not yet been realized due to crucial challenges that remain in the field. In particular, the development of nanoparticles with new plasmonic properties and surface chemistries could enable the rational design of more complex architectures capable of performing advanced functions, like cascade reactions, energy conversion, or signal transduction. The scope of this short review is to highlight the most recent developments in the synthesis and self-assembly of anisotropic metal nanoparticles, which are capable of bringing forward the next generation of plasmonic materials.


2005 ◽  
Vol 88 (2) ◽  
pp. 101-131 ◽  
Author(s):  
Martinus H.V. Werts

The luminescence of trivalent lanthanide ions has found applications in lighting, lasers, optical telecommunications, medical diagnostics, and various other fields. This introductory review presents the basics of organic and inorganic luminescent materials containing lanthanide ions, their applications, and some recent developments. After a brief history of the discovery, purification and early spectroscopic studies of the lanthanides, the radiative and nonradiative transitions of the 4f electrons in lanthanide ions are discussed. Lanthanide-doped phosphors, glasses and crystals as well as luminescent lanthanide complexes with organic ligands receive attention with respect to their preparation and their applications. Finally, two recent developments in the field of luminescent materials are addressed: near-infrared luminescent lanthanide complexes and lanthanide-doped nanoparticles.


Synthesis ◽  
2017 ◽  
Vol 49 (15) ◽  
pp. 3337-3346 ◽  
Author(s):  
Manabu Abe ◽  
Youhei Chitose ◽  
Satish Jakkampudi ◽  
Pham Thuy ◽  
Qianghua Lin ◽  
...  

Near-infrared two-photon (TP)-induced photorelease (uncaging) of bioactive molecules such as drugs has attracted considerable attention because of its ability to elucidate mechanistic aspects of biological processes. This short review summarizes recent developments in the design and synthesis of TP-responsive chromophores.1 Introduction2 Molecular Design of TP-Responsive Organic Chromophores for ‘Caging & Uncaging’2.1 π-Conjugation2.2 A Dipolar System2.3 A Quadrupolar System2.4 An Octupolar System3 Recent Developments of TP Uncaging Reactions3.1 4-Methoxy-7-nitroindolinyl Caged Auxins3.2 Uncaging of GABA and Tryptophan Using TP-Induced Electron-Transfer Reactions3.3 Effect of Position Isomery in Aminoquinoline-Derived Photolabile Protecting Groups (PPGs)3.4 Cooperative Dyads for TP Uncaging3.5 Caged Calcium with a Bis-styrylthiophene Backbone3.6 Cloaked Caged Compounds3.7 Three-Dimensional Control of DNA Hybridization by Orthogonal Two-Color TP Uncaging3.8 TP-Induced Release of Diethyl Phosphate (DEP) and ATP4 Our Contribution to TP Uncaging Reactions5 Summary


2011 ◽  
Vol 64 (5) ◽  
pp. 519 ◽  
Author(s):  
Zhe Sun ◽  
Jishan Wu

Higher order acenes and fused acenes represent two outstanding classes of building blocks to achieve near-infrared absorbing and emitting materials. Appropriate chemical modification and functionalization will lead to significant improvements in solubility and stability, thus making their applications practically possible. This short review summarizes the recent developments of the two types of polycyclic aromatic compounds mentioned above based on their physical and optical properties including absorption, emission, quantum yield, solubility, and stability.


2012 ◽  
Vol 727-728 ◽  
pp. 1913-1918 ◽  
Author(s):  
H.C. Silva ◽  
Crislene Rodrigues da Silva Morais ◽  
S.A. Morais ◽  
B.F. Lira

The coordination of lanthanide íons with organic ligands has provided good luminescent properties and allows its application in molecular light converter devices, which motivates the scientific interest of seeking coordination of these íons with organic ligands that potentiate the luminescence and associate biological properties of the complexes formed. From this perspective the complex was synthesized Eu (III) with mesoionic 2(4-chlorophenyl)-3-methyl (methoxyphenyl)-1,3-thiazole-5-thiolate (MS-1) and bipy, with the aim of its possible application in the areas of photoluminescence and drug. Analyses were performed using TG, DSC, XRD and IR. The complex obtained after reaction of the lanthanide salt and organic ligands showed five stages of decomposition and different fusion of the isolated ligands.


2015 ◽  
Vol 6 (1) ◽  
pp. 457-471 ◽  
Author(s):  
Oxana Kotova ◽  
Salvador Blasco ◽  
Brendan Twamley ◽  
John O'Brien ◽  
Robert D. Peacock ◽  
...  

The binding of asymmetrical and optically pure tridentate ligands containing one carboxylic group and 2-naphthyl as an antenna to lanthanide ions was studied in CH3CN.


2013 ◽  
Vol 20 (12) ◽  
pp. 1595-1608 ◽  
Author(s):  
D. Fernandez ◽  
I. Pallares ◽  
G. Covaleda ◽  
F. X. Aviles ◽  
J. Vendrell

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