Literature DB >> 20945840

Hexa boron-dipyrromethene cyclotriphosphazenes: synthesis, crystal structure, and photophysical properties.

M Rajeswara Rao1, R Bolligarla, Ray J Butcher, M Ravikanth.   

Abstract

We have synthesized four examples of a cyclotriphosphazene ring appended with six boron-dipyrromethene dyes N(3)P(3)(BODIPY)(6) by adopting two different methods. In method I, 1 equiv of N(3)P(3)Cl(6) was treated with 6 equiv of meso-(o- or m- or p-hydroxyphenyl)boron-dipyrromethene in tetrahydrofuran (THF) in the presence of cesium carbonate. This afforded N(3)P(3)(BODIPY)(6) in yields ranging from 80 to 90%. In method II, we first prepared hexakis(p-formylphenoxy)cyclotriphosphazene N(3)P(3)(CHO)(6) by treating 1 equiv of N(3)P(3)Cl(6) with 6 equiv of 4-hydroxybenzaldehyde in the presence of cesium carbonate in THF. In the second step, N(3)P(3)(CHO)(6) was condensed with excess of pyrrole in the presence of catalytic amount of trifluoroacetic acid (TFA) in CH(2)Cl(2) at room temperature and afforded hexakis(p-phenoxy dipyrromethane)cyclotriphosphazene. In the last step, the hexakis(p-phenoxy dipyrromethane)cyclotriphosphazene was first oxidized with 6 equiv of DDQ in CH(2)Cl(2) at room temperature for 1 h followed by neutralization with triethylamine and further reaction with excess BF(3)·Et(2)O afforded the target N(3)P(3)(BODIPY)(6) in 16% yield. The route II was used only for the synthesis of one target compound whereas the route I was used for the synthesis of all four target compounds. The four compounds were characterized by mass, NMR, absorption, electrochemical, and fluorescence techniques. The crystal structure solved for one of the compounds revealed that the P(3)N(3) ring is slightly puckered and the six substituents were not interacting with each other and attained pseudo-axial and pseudo-equatorial positions. The photophysical studies in five different solvents indicated that the compounds exhibit large Stokes' shifts unlike reference monomeric BODIPYs indicating that the compounds are promising for fluorescence bioassays. The quantum yields and lifetimes of compounds 1-4 depends on the type of BODIPY unit attached to the cyclotriphosphazene ring.

Entities:  

Year:  2010        PMID: 20945840     DOI: 10.1021/ic1016092

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  5 in total

1.  Rationally Designed Fluorescent pH Sensors for Measurements in Extremely Alkaline Media.

Authors:  Nurcan Tuncer; Efdal Teknikel; Canan Unaleroglu
Journal:  J Fluoresc       Date:  2018-10-18       Impact factor: 2.217

2.  Study on the Synthesis, Photophysical Properties and Singlet Oxygen Generation Behavior of Bodipy-Functionalized Cyclotriphosphazenes.

Authors:  Elif Şenkuytu; Zeynep Cebesoy; Gönül Yenilmez Çiftçi; Esra Tanrıverdi Eçik
Journal:  J Fluoresc       Date:  2016-11-16       Impact factor: 2.217

3.  Novel Coumarin Substituted Water Soluble Cyclophosphazenes as "Turn-Off" Type Fluorescence Chemosensors for Detection of Fe(3+) ions in Aqueous Media.

Authors:  Gönül Yenilmez Çiftçi; Elif Şenkuytu; Mustafa Bulut; Mahmut Durmuş
Journal:  J Fluoresc       Date:  2015-09-29       Impact factor: 2.217

4.  Novel Water-Soluble Cyclotriphosphazene-Bodipy Conjugates: Synthesis, Characterization and Photophysical Properties.

Authors:  Seda Çetindere; Elif Okutan; Süreyya Oğuz Tümay; Serkan Yeşilot; Adem Kılıç
Journal:  J Fluoresc       Date:  2019-08-13       Impact factor: 2.217

5.  Pyrene-BODIPY-substituted novel water-soluble cyclotriphosphazenes: synthesis, characterization, and photophysical properties.

Authors:  Seda Çetİndere; Serkan YeŞİlot; Adem KiliÇ
Journal:  Turk J Chem       Date:  2020-02-11       Impact factor: 1.239

  5 in total

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