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Items: 1 to 20 of 101

1.

Synthesis and Optoelectrical Characterization of Novel Squaraine Dyes Derived from Benzothiophene and Benzofuran.

Rao GH, Pandey M, Narayanaswamy K, Srinivasa Rao R, Pandey SS, Hayase S, Singh SP.

ACS Omega. 2018 Oct 23;3(10):13919-13927. doi: 10.1021/acsomega.8b01240. eCollection 2018 Oct 31.

2.

Application of solution processable squaraine dyes as electron donors for organic bulk-heterojunction solar cells.

Rao BA, Yesudas K, Kumar GS, Bhanuprakash K, Rao VJ, Sharma GD, Singh SP.

Photochem Photobiol Sci. 2013 Sep;12(9):1688-99. doi: 10.1039/c3pp50087j.

PMID:
23788052
3.

n-Channel semiconductor materials design for organic complementary circuits.

Usta H, Facchetti A, Marks TJ.

Acc Chem Res. 2011 Jul 19;44(7):501-10. doi: 10.1021/ar200006r. Epub 2011 May 26.

PMID:
21615105
4.

Effect of Out-of-Plane Alkyl Group's Position in Dye-Sensitized Solar Cell Efficiency: A Structure-Property Relationship Utilizing Indoline-Based Unsymmetrical Squaraine Dyes.

Alagumalai A, M K MF, Vellimalai P, Sil MC, Nithyanandhan J.

ACS Appl Mater Interfaces. 2016 Dec 28;8(51):35353-35367. doi: 10.1021/acsami.6b12730. Epub 2016 Dec 13.

PMID:
27957855
5.

Thieno[3,4-b]thiophene-Based Novel Small-Molecule Optoelectronic Materials.

Zhang C, Zhu X.

Acc Chem Res. 2017 Jun 20;50(6):1342-1350. doi: 10.1021/acs.accounts.7b00050. Epub 2017 Apr 4.

6.

Linear and nonlinear optical characterizations of a monomeric symmetric squaraine-based dye in solution.

Toro C, De Boni L, Yao S, Ritchie JP, Masunov AE, Belfield KD, Hernandez FE.

J Chem Phys. 2009 Jun 7;130(21):214504. doi: 10.1063/1.3147011.

PMID:
19508073
7.

High-performance organic thin-film transistors of J-stacked squaraine dyes.

Gsänger M, Kirchner E, Stolte M, Burschka C, Stepanenko V, Pflaum J, Würthner F.

J Am Chem Soc. 2014 Feb 12;136(6):2351-62. doi: 10.1021/ja409496r. Epub 2014 Jan 30.

PMID:
24432873
8.

Squaraine Dyes: Molecular Design for Different Applications and Remaining Challenges.

Ilina K, MacCuaig WM, Laramie M, Jeouty JN, McNally LR, Henary M.

Bioconjug Chem. 2019 Aug 12. doi: 10.1021/acs.bioconjchem.9b00482. [Epub ahead of print]

PMID:
31365819
9.

Synthesis, vibrational spectroscopy and X-ray structural characterization of novel NIR emitter squaramides.

Ávila-Costa M, Donnici CL, Dos Santos JD, Diniz R, Barros-Barbosa A, Cuin A, de Oliveira LFC.

Spectrochim Acta A Mol Biomol Spectrosc. 2019 Dec 5;223:117354. doi: 10.1016/j.saa.2019.117354. Epub 2019 Jul 8.

PMID:
31323496
10.

Supramolecular adducts of squaraine and protein for noninvasive tumor imaging and photothermal therapy in vivo.

Gao FP, Lin YX, Li LL, Liu Y, Mayerhöffer U, Spenst P, Su JG, Li JY, Würthner F, Wang H.

Biomaterials. 2014 Jan;35(3):1004-14. doi: 10.1016/j.biomaterials.2013.10.039. Epub 2013 Oct 26.

PMID:
24169004
11.

Properties of electronically excited states of four squaraine dyes and their complexes with fullerene C70: A theoretical investigation.

Zhang J, Li T.

Spectrochim Acta A Mol Biomol Spectrosc. 2017 Sep 5;184:82-88. doi: 10.1016/j.saa.2017.04.086. Epub 2017 May 1.

PMID:
28486203
12.

Bithiophene-imide-based polymeric semiconductors for field-effect transistors: synthesis, structure-property correlations, charge carrier polarity, and device stability.

Guo X, Ortiz RP, Zheng Y, Hu Y, Noh YY, Baeg KJ, Facchetti A, Marks TJ.

J Am Chem Soc. 2011 Feb 9;133(5):1405-18. doi: 10.1021/ja107678m. Epub 2011 Jan 5.

PMID:
21207965
13.

Arylamine-based squaraine donors for use in organic solar cells.

Wei G, Xiao X, Wang S, Zimmerman JD, Sun K, Diev VV, Thompson ME, Forrest SR.

Nano Lett. 2011 Oct 12;11(10):4261-4. doi: 10.1021/nl2022515. Epub 2011 Sep 22.

PMID:
21923102
14.

Precise Side-Chain Engineering of Thienylenevinylene-Benzotriazole-Based Conjugated Polymers with Coplanar Backbone for Organic Field Effect Transistors and CMOS-like Inverters.

Lee MH, Kim J, Kang M, Kim J, Kang B, Hwang H, Cho K, Kim DY.

ACS Appl Mater Interfaces. 2017 Jan 25;9(3):2758-2766. doi: 10.1021/acsami.6b14701. Epub 2017 Jan 9.

PMID:
28004581
15.

Bovine serum albumin nanoparticles with fluorogenic near-IR-emitting squaraine dyes.

Zhang Y, Yue X, Kim B, Yao S, Bondar MV, Belfield KD.

ACS Appl Mater Interfaces. 2013 Sep 11;5(17):8710-7. doi: 10.1021/am402361w. Epub 2013 Aug 30.

16.

Novel A2-D-A1-D-A2 type NIR absorbing symmetrical squaraines based on 2, 3, 3, 8-tetramethyl-3H-pyrrolo [3, 2-h] quinoline: Synthesis, photophysical, electrochemical, thermal properties and photostability study.

Khopkar S, Jachak M, Shankarling G.

Spectrochim Acta A Mol Biomol Spectrosc. 2019 Mar 15;211:114-124. doi: 10.1016/j.saa.2018.11.061. Epub 2018 Nov 30.

PMID:
30530063
17.

Molecular Engineering and Structure-Related Properties of Squaraine Dyes Based on the Core and Wings Concept.

Rao GH, Rana PJS, Chitumalla RK, Jang J, Singh SP.

ACS Omega. 2018 Nov 13;3(11):15416-15425. doi: 10.1021/acsomega.8b01809. eCollection 2018 Nov 30.

18.
19.

A comparative study of semi-squaraine and squaraine dyes using computational techniques: tuning the charge transfer/biradicaloid character by substitution.

Puyad AL, Chaitanya GK, Prabhakar C, Bhanuprakash K.

J Mol Model. 2013 Jan;19(1):275-87. doi: 10.1007/s00894-012-1543-8. Epub 2012 Aug 10.

PMID:
22878861
20.

A Quinacridone-Diphenylquinoxaline-Based Copolymer for Organic Field-Effect Transistors.

Jeong YJ, Oh JH, Song HJ, An TK.

Polymers (Basel). 2019 Mar 26;11(3). pii: E563. doi: 10.3390/polym11030563.

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