scholarly journals Near-infrared 2Eg → 4A2g and visible LMCT luminescence from a molecular bis-(tris(carbene)borate) manganese(IV) complex

2017 ◽  
Vol 95 (5) ◽  
pp. 547-552 ◽  
Author(s):  
Joe P. Harris ◽  
Christian Reber ◽  
Hannah E. Colmer ◽  
Timothy A. Jackson ◽  
Adam P. Forshaw ◽  
...  

The molecular bis-(tris(carbene)borate) manganese(IV) complex [{PhB(MeIm)3}2Mn](OTf)2 shows 2Eg → 4A2g luminescence at 828 nm in the solid state at 85 K; this wavelength is longer by approximately 100 nm than the wavelengths typically observed for manganese(IV) and chromium(III) doped solids and for molecular chromium(III) complexes. Weak luminescence is also observed from a LMCT excited state with an absorption maximum at 500 nm. This represents the first molecular manganese(IV) compound for which luminescence has been reported.

2015 ◽  
Vol 3 (19) ◽  
pp. 4910-4920 ◽  
Author(s):  
Jia-Ling Liao ◽  
Yun Chi ◽  
Chia-Chi Yeh ◽  
Hao-Che Kao ◽  
Chih-Hao Chang ◽  
...  

Os(ii) complexes bearing chromophoric 1,10-phenanthroline, diphosphine and bipyrazolate ancillaries display efficient NIR emission ranging from 717 nm to 779 nm in the solid state at RT.


ACS Omega ◽  
2018 ◽  
Vol 3 (10) ◽  
pp. 14341-14348 ◽  
Author(s):  
Abhishek Kumar Gupta ◽  
Ashwani Kumar ◽  
Ranjit Singh ◽  
Manisha Devi ◽  
Abhimanew Dhir ◽  
...  

2019 ◽  
Author(s):  
Haoke Zhang ◽  
Lili Du ◽  
Lin Wang ◽  
Junkai Liu ◽  
Qing Wan ◽  
...  

<p>Building molecular machine has long been a dream of scientists as it is expected to revolutionize many aspects of technology and medicine. Implementing the solid-state molecular motion is the prerequisite for a practical molecular machine. However, few works on solid-state molecular motion have been reported and it is almost impossible to “see” the motion even if it happens. Here the light-driven molecular motion in solid state is discovered in two non-conjugated molecules <i>s</i>-DPE and <i>s</i>-DPE-TM, resulting in the formation of excited-state though-space complex (ESTSC). Meanwhile, the newly formed ESTSC generates an abnormal visible emission which is termed as clusteroluminescence. Notably, the original packing structure can recover from ESTSC when the light source is removed. These processes have been confirmed by time-resolved spectroscopy and quantum mechanics calculation. This work provides a new strategy to manipulate and “see” solid-state molecular motion and gains new insights into the mechanistic picture of clusteroluminescence.<br></p>


Author(s):  
Fabrice Pointillart ◽  
Bertrand Lefeuvre ◽  
Carlo Andrea Mattei ◽  
Jessica Flores Gonzalez ◽  
Frédéric Gendron ◽  
...  

2021 ◽  
Author(s):  
xiudi wu ◽  
shuang zhao ◽  
Liang Zhang ◽  
Langping Dong ◽  
Yonghui Xu ◽  
...  

Abstract:Gd2GaSbO7:Cr3+,Yb3+ phosphors with efficient broadband NIR emission were prepared by solid-state reaction. Under the excitation of 448 nm, Gd2GaSbO7:Cr3+ (GGS:Cr3+) phosphor exhibits a broadband NIR emission band centered at approximately...


2021 ◽  
pp. 2001947
Author(s):  
Reiko Aoki ◽  
Ryutaro Komatsu ◽  
Kenichi Goushi ◽  
Masashi Mamada ◽  
Soo Young Ko ◽  
...  

2005 ◽  
Vol 59 (11) ◽  
pp. 1393-1398 ◽  
Author(s):  
Reikichi Iwamoto ◽  
Akishi Nara ◽  
Toshihiko Matsuda

In the present report we studied spectral characteristics of the near-infrared combination and overtone bands of CH vibrations of a CH sequence. The near-infrared bands of the CH in CHX3 (X, halogen), which were interpreted in terms of the CH stretching and CH deformation fundamentals without any ambiguity, typically showed how the frequency and intensity of a combination or an overtone depend on the vibrational excited state. In the CH–C–CH of CHX2CX2CHX2, the vibrations of one CH are isolated from those of the other CH, and the combination and overtone bands were similarly interpreted as those of the CH, although each of the combination bands was split into two because of non-degeneracy of the CH deformation. In the CH–CH of CHX2CHX2, the CH deformations only have coupled modes. The first combination showed four narrowly separate bands, which were reasonably interpreted on the basis of the CH stretching and the coupled CH deformation modes. We demonstrated that the first combination of coupled modes as well as the combination of up to, at least, the third order of isolated modes have the nature of the characteristic bands.


2016 ◽  
Vol 4 (16) ◽  
pp. 3599-3606 ◽  
Author(s):  
Toshiki Mutai ◽  
Tatsuya Ohkawa ◽  
Hideaki Shono ◽  
Koji Araki

The color of ESIPT luminescence of HPIP is tuned in a wide range by the introduction of aryl group(s), and thus a series of PIPs showing blue to red emission is realized.


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