A highly versatile fluorenone-based macrocycle for the sensitive detection of polycyclic aromatic hydrocarbons and fluoride anions

Ingrid Suzy Tamgho; Sauradip Chaudhuri; Molly Verderame; Dana J. DiScenza; Mindy Levine

doi:10.1039/c7ra05404a

A highly versatile fluorenone-based macrocycle for the sensitive detection of polycyclic aromatic hydrocarbons and fluoride anions

Ingrid Suzy Tamgho
, Sauradip Chaudhuri
, Molly Verderame
, Dana J. DiScenza
, Mindy Levine

نتاج البحث: نشر في مجلة › مقالة › مراجعة النظراء

17 اقتباسات (Scopus)

ملخص

Reported herein is the high yielding synthesis of a new fluorenone-based triazolophane and its sensing capabilities for polycyclic aromatic hydrocarbons (PAHs) and fluoride anions. Fluorescence, UV/Vis and ¹H NMR spectroscopy results showed the triazolophane has a high sensitivity for selected PAHs and binds the fluoride anion in a 2:1 stoichiometry via C-H hydrogen bonding with the triazole and fluorenone protons.

اللغة الأصلية	الإنجليزيّة
الصفحات (من إلى)	28489-28493
عدد الصفحات	5
دورية	RSC Advances
مستوى الصوت	7
رقم الإصدار	45
المعرِّفات الرقمية للأشياء	https://doi.org/10.1039/c7ra05404a
حالة النشر	نُشِر - 2017
منشور خارجيًا	نعم

الوصول إلى المستند

10.1039/c7ra05404a

الملفات والروابط الأخرى

Link to publication in Scopus

قم بذكر هذا

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title = "A highly versatile fluorenone-based macrocycle for the sensitive detection of polycyclic aromatic hydrocarbons and fluoride anions",

abstract = "Reported herein is the high yielding synthesis of a new fluorenone-based triazolophane and its sensing capabilities for polycyclic aromatic hydrocarbons (PAHs) and fluoride anions. Fluorescence, UV/Vis and 1H NMR spectroscopy results showed the triazolophane has a high sensitivity for selected PAHs and binds the fluoride anion in a 2:1 stoichiometry via C-H hydrogen bonding with the triazole and fluorenone protons.",

author = "Tamgho, \{Ingrid Suzy\} and Sauradip Chaudhuri and Molly Verderame and DiScenza, \{Dana J.\} and Mindy Levine",

note = "Publisher Copyright: {\textcopyright} 2017 The Royal Society of Chemistry.",

year = "2017",

doi = "10.1039/c7ra05404a",

language = "אנגלית",

volume = "7",

pages = "28489--28493",

journal = "RSC Advances",

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TY - JOUR

T1 - A highly versatile fluorenone-based macrocycle for the sensitive detection of polycyclic aromatic hydrocarbons and fluoride anions

AU - Tamgho, Ingrid Suzy

AU - Chaudhuri, Sauradip

AU - Verderame, Molly

AU - DiScenza, Dana J.

AU - Levine, Mindy

PY - 2017

Y1 - 2017

N2 - Reported herein is the high yielding synthesis of a new fluorenone-based triazolophane and its sensing capabilities for polycyclic aromatic hydrocarbons (PAHs) and fluoride anions. Fluorescence, UV/Vis and 1H NMR spectroscopy results showed the triazolophane has a high sensitivity for selected PAHs and binds the fluoride anion in a 2:1 stoichiometry via C-H hydrogen bonding with the triazole and fluorenone protons.

AB - Reported herein is the high yielding synthesis of a new fluorenone-based triazolophane and its sensing capabilities for polycyclic aromatic hydrocarbons (PAHs) and fluoride anions. Fluorescence, UV/Vis and 1H NMR spectroscopy results showed the triazolophane has a high sensitivity for selected PAHs and binds the fluoride anion in a 2:1 stoichiometry via C-H hydrogen bonding with the triazole and fluorenone protons.

UR - https://www.scopus.com/pages/publications/85021692629

U2 - 10.1039/c7ra05404a

DO - 10.1039/c7ra05404a

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:85021692629

SN - 2046-2069

VL - 7

SP - 28489

EP - 28493

JO - RSC Advances

JF - RSC Advances

IS - 45

ER -

A highly versatile fluorenone-based macrocycle for the sensitive detection of polycyclic aromatic hydrocarbons and fluoride anions

ملخص

الوصول إلى المستند

الملفات والروابط الأخرى

بصمة

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