Work in Bunz's laboratory at the Georgia Institute of Technology was supported in part by the National Science Foundation (NSF-CHE 07502753) and the work at Ruprecht-Karls-Universit&auml;t Heidelberg was funded by the "Struktur und Innovationsfond des Landes Baden-W&uuml;rttemberg". Work in Miljani&#263;'s laboratory at the University of Houston was funded by the National Science Foundation CAREER program (CHE-1151292), the Welch Foundation (grant no. E-1768), the University of Houston (UH) and its Small Grant program, and the Texas Center for Superconductivity at UH.

1. Detection of Carboxylic Acids Using Distyrylbis(arylethynyl)benzene Cruciforms
<ol>
	<li>Prepare a fresh stock solution of cruciforms 1-3 with a concentration of 1.0 x 10-3 mol/L in DCM. It is not necessary to use spectroscopic quality solvents; ACS reagent grade purity is sufficient.</li>
	<li>Using the stock solutions from 1.1 prepare 100 ml each of 2.0 x 10-6 M solution of 1-3 in dichloromethane (DCM), ethyl acetate (EtOAc), acetonitrile (AN), N,N-dimethylformamide (DMF), isopropyl alcohol (iPrOH) and methanol (MeOH). It is not necessary to use spectroscopic quality solvents; ACS reagent grade purity is sufficient.</li>
	<li>Weigh out 0.65 mmol (88.2-124.2 mg) of the analyte carboxylic acid A1 - A10 in 5 ml dram vials, add 5 ml of the solutions prepared in 2.1 and shake the vial. If heterogeneous, the corresponding solution should be left to settle (filtration is unnecessary).This leads to a total concentration of 0.13 M (31 g/L) of the carboxylic acid.</li>
	<li>Capture digital photographs of the fluorescence in a dark room in the absence of ambient light. The photographic setup (Figure 2) includes a digital camera (Canon EOS 30D) equipped with an objective (EFS 18-55 mm zoom lens) and two UV-lamps (excitation wavelength 365 nm). The uncapped vials should be positioned under the two UV-lamps for maximum exposure with a distance of 60 cm between camera lens and sample vials. Exposure times were varied for each solution to produce images reflecting the color of emission (0.25 - 15 sec).</li>
</ol>
2. Detection of Boronic Acids Using Benzobisoxazole Cruciforms
<ol>
	<li>Prepare a 1.0 x 10-4 M solution of cruciform 4 in DCM. It is not necessary to use spectroscopic quality solvent; ACS reagent grade purity is sufficient.</li>
	<li>Prepare five individual solutions for each boronic acid analyte, by dissolving 50 mg (0.24-0.41 mmol) of the analyte in 3 ml each of acetonitrile (AN), 1,2,4-trichlorobenzene (TCB), dichloromethane (DCM), cyclohexane (CH), and chlorobenzene (CB). This should result in approx. 16.7 g/L solutions with respect to each analyte. It is not necessary to use spectroscopic quality solvents; ACS reagent grade purity is sufficient.</li>
	<li>Transfer 1.8 ml of each of the analyte solutions prepared in 2.2 into five separate 10 x 10 mm quartz cuvettes (commonly used for UV/Vis spectroscopy). Then, add 20 &#956;l of the cruciform solution prepared in 2.1 into each of the five cuvettes, and stir the two solutions to homogenize. If any precipitation is observed, the corresponding solution should simply be left to settle (filtration is unnecessary).</li>
	<li>Place all five cuvettes onto a glass plate and irradiate them by a handheld UV lamp (365 nm) from the top. The UV lamp should be positioned in a fashion that ensures equal irradiation to all five vials.</li>
	<li>Ensure that the room is dark (turn off lights, block windows and other sources of natural and artificial light) and immediately take a digital photograph of the emission colors of the solutions. Miljani&#263; et al. have used two digital camera models: FujiFilm FinePix S9000 and Canon EOS Rebel T3i, with a 45 cm distance between the camera lens and the sample cuvettes. Shutter speed was 0.5 sec.</li>
</ol>
3. Detection of Amine Analytes Using Benzobisoxazole Cruciform/Boronic Acids Hybrid Sensing System
<ol>
	<li>Prepare (at least) 80 ml each of 1.0 x 10-6 M solutions of cruciform 4 in acetonitrile (AN), 1,2,4-trichlorobenzene (TCB), cyclohexane (CH), dichloromethane (DCM), and chloroform (CF).</li>
	<li>Dissolve B1 (152.6 mg, 0.80 mmol) in 40 ml of each of the solutions prepared in 3.1.</li>
	<li>Dissolve B5 (97.6 mg, 0.80 mmol) in 40 ml of each of the solutions prepared in 3.1.</li>
	<li>Immediately after the solutions described in 3.2 and 3.3 are prepared, use them (2 ml each) to dissolve the desired amine analyte (40 mg, 0.19-0.47 mmol). For each amine analyte, ten solutions should be prepared: five with B1 and five with B5 as additives. It is not necessary to use spectroscopic quality solvents; ACS reagent grade purity is sufficient.</li>
	<li>For each analyte, transfer aliquots of the ten prepared analyte/boronic acid/cruciform 4 solutions into ten separate quartz cuvettes. Place these two five-cuvette sets (one for 4/B1, one for 4/B5) onto a glass plate, irradiate at 365 nm by a handheld UV lamp, and immediately photograph using the settings described in 2.5 above.</li>
</ol>
4. Image Processing and Numeric Analyte Discrimination
<ol>
	<li>Using Adobe PhotoShop or a similar image-processing program, cut out a representative square segment from digital photographs of the emission colors of each photographed vial. Organize these cut-outs into panels similar to those in Figures 3B, 4, and 5. These panels in many cases allow rapid naked-eye discrimination among analytes.</li>
	<li>If quantification of differences in emission color is desired, R/G/B values can be extracted from panels in 4.1 and then statistically treated. Freely downloadable Colour Contrast Analyzer14 can be used for this purpose. To obtain relative standard deviations of emission colors of one analyte relative to another (e.g. compounds B1 and B2, Figure 4), the following equation is used: 
	<img alt="Equation 1" src="/files/ftp_upload/50858/50858eq1.jpg" /></li>
	<li>The equation from 4.2 is also used to identify unknown carboxylic acid analytes. Therefore every deviation is determined between the unknown analyte to all substances of the calibration data set. The smallest deviation indicates the corresponding substance.</li>
</ol>

<ol>
	<li>Zucchero, A. J., McGrier, P. J., Bunz, U. H. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cross-conjugated+cruciform+fluorophores.">Cross-conjugated cruciform fluorophores.</a> Acc. Chem. Res. 43 (3), 397-408 (2010).</li><li>Feldman, A. K., Steigerwald, M. L., Guo, X., Nuckolls, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Molecular+electronic+devices+based+on+single-walled+carbon+nanotube+electrodes.">Molecular electronic devices based on single-walled carbon nanotube electrodes.</a> Acc. Chem. Res. 41 (12), 1731-1741 (2008).</li><li>Galbrecht, F., B&#252;nnagel, T., Bilge, A., Scherf, T. J. J., M&#252;ller, U. H. F., Bunz, <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Functional Organic Materials. , 83 (2007).</li><li>Marsden, J. A., Miller, J. J., Shirtcliff, L. D., Haley, M. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Structure-property+relationships+of+donor/acceptor-functionalized+tetrakis(phenylethynyl)benzenes+and+bis(dehydrobenzoannuleno)+benzenes.">Structure-property relationships of donor/acceptor-functionalized tetrakis(phenylethynyl)benzenes and bis(dehydrobenzoannuleno) benzenes.</a> J. Am. Chem. Soc. 127 (8), 2464-2476 (2005).</li><li>Lim, J., Albright, T. A., Martin, B. R., Miljani&#263;, O. &. #. 3. 5. 2. ;. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Benzobisoxazole+cruciforms:+heterocyclic+fluorophores+with+spatially+separated+frontier+molecular+orbitals.">Benzobisoxazole cruciforms: heterocyclic fluorophores with spatially separated frontier molecular orbitals.</a> J. Org. Chem. 76 (24), 10207-10219 (2011).</li><li>Lirag, R. C., Le, H. T. M., Miljani&#263;, O. &. #. 3. 5. 2. ;. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=L-shaped+benzimidazole+fluorophores:+synthesis,+characterization+and+optical+response+to+bases,+acids+and+anions.">L-shaped benzimidazole fluorophores: synthesis, characterization and optical response to bases, acids and anions.</a> Chem. Commun. , (2013).</li><li>Hauck, M., Schoenhaber, J., Zucchero, A. J., Hardcastle, K. I., Mueller, T. J. J., Bunz, U. H. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phenothiazine+cruciforms:+synthesis+and+metallochromic+properties.">Phenothiazine cruciforms: synthesis and metallochromic properties.</a> J. Org. Chem. 72 (18), 6714-6725 (2007).</li><li>Zucchero, A. J., Wilson, J. N., Bunz, U. H. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cruciforms+as+functional+fluorophores:+response+to+protons+and+selected+metal+ions.">Cruciforms as functional fluorophores: response to protons and selected metal ions.</a> J. Am. Chem. Soc. 128 (36), 11872-11881 (2006).</li><li>Wilson, J. N., Bunz, U. H. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Switching+of+intramolecular+charge+transfer+in+cruciforms:+metal+ion+sensing.">Switching of intramolecular charge transfer in cruciforms: metal ion sensing.</a> J. Am. Chem. Soc. 127 (12), 4124-4125 (2005).</li><li>Davey, E. A., Zucchero, A. J., Trapp, O., Bunz, U. H. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Discrimination+of+organic+acids+using+a+three+molecule+array+based+upon+cruciform+fluorophores.">Discrimination of organic acids using a three molecule array based upon cruciform fluorophores.</a> J. Am. Chem. Soc. 133 (20), 7716-7718 (2011).</li><li>Lim, J., Nam, D., Miljani&#263;, O. &. #. 3. 5. 2. ;. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Identification+of+carboxylic+and+organoboronic+acids+and+phenols+with+a+single+benzobisoxazole+fluorophore.">Identification of carboxylic and organoboronic acids and phenols with a single benzobisoxazole fluorophore.</a> Chem. Sci. 3 (2), 559-563 (2012).</li><li>Lim, J., Miljani&#263;, O. &. #. 3. 5. 2. ;. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Benzobisoxazole+fluorophore+vicariously+senses+amines,+ureas,+anions.">Benzobisoxazole fluorophore vicariously senses amines, ureas, anions.</a> Chem. Commun. 48 (83), 10301-10303 (2012).</li><li>Braga, D., Polito, M., Bracaccini, M., D'Addario, D., Tagliavini, E., Sturba, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Novel+organometallic+building+blocks+for+molecular+crystal+engineering.+2.+Synthesis+and+characterization+of+pyridyl+and+pyrimidyl+derivatives+of+diboronic+acid,+Fe(&#951;5-C5H4+-+B(OH)2)2],+and+of+pyridyl+boronic+acid,+[Fe(&#951;5-C5H4-4-C5H4N)(&#951;5-C5H4+-+B(OH)2)].">Novel organometallic building blocks for molecular crystal engineering. 2. Synthesis and characterization of pyridyl and pyrimidyl derivatives of diboronic acid, Fe(&#951;5-C5H4 - B(OH)2)2], and of pyridyl boronic acid, [Fe(&#951;5-C5H4-4-C5H4N)(&#951;5-C5H4 - B(OH)2)].</a> Organometallics. 22 (10), 2142-2150 (2003).</li><li>Schwaebel, T., Trapp, O., Bunz, U. H. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Digital+photography+for+the+analysis+of+fluorescence+responses.">Digital photography for the analysis of fluorescence responses.</a> Chem. Sci. 4 (3), 273-281 (2013).</li></ol>

We have nothing to disclose.

The protocols for qualitative discrimination described in this paper and video hold significant potential in routine quality analyses, where even a minimally trained operator could discern the differences in composition, or deviations from a well-defined formula. Practicality of this technique could be further enhanced by using simple cellphone cameras, which, in combination with pattern- and image-recognition software such as Google Goggles, could match the recorded emission colors to the database of known compositions....

Molecular cruciforms are defined as X-shaped cross-conjugated molecules in which two conjugation circuits intersect at a central core.1,2,3 With appropriate donor-acceptor substitution, these molecules can spatially localize their frontier molecular orbitals (FMOs), so that the highest occupied molecular orbital (HOMO) resides dominantly along the electron-rich axis of the molecule, while the lowest unoccupied molecular orbital (LUMO) has the bulk of its density positioned along the electron-poor arm of the molecule. Such spatial isolation of FMOs is essential in the applications of these cruciforms as sensors for small molecules, since analyte binding to the cruciform invariably changes its HOMO-LUMO gap and the associated optical properties. This behavior has been demonstrated in cruciforms based on 1,4-distyryl-2,5-bis(arylethynyl)benzene,1 1,2,4,5-tetrakisethynylbenzene,4 and benzobisoxazole5,6 structural motifs. Since all three classes of molecules are inherently fluorescent, this methodology allowed their use as small-molecule sensors. In all three examples, cruciforms were substituted with Lewis basic pyridine and dialkylaniline groups and were thus responsive to Lewis acidic analytes, such as protons and metal ions.1,4,5,7,8,9
In 2011, Bunz and coworkers have shown10 that the fluorescence responses of 1,4-distyryl-2,5-bis(arylethynyl)benzene cruciforms 1 - 3 (Figure 1) dramatically varied depending on the structure of the carboxylic acid used to induce protonation of the cruciform. Subsequently, Miljani&#263; et al. demonstrated that benzobisoxazole cruciforms such as 4 (Figure 1) also show highly specific fluorescence emission responses to structurally related carboxylic acids, and that similar distinction can be seen among very similar organoboronic acids, too.11 Origins of this highly selective emission color changes are at present unclear, and are most likely complex - as fluorescence quenching by electron poor analytes, residual analyte fluorescence, and protonation-induced shifting of cruciforms&#39; emission maxima all presumably play a role. Nevertheless, the ability to discriminate among structurally related analytes is significant, especially since statistically relevant distinction can be obtained without the need to perform exhaustive UV/Vis absorption or fluorescence characterization of the optical response of cruciforms to analytes. Instead, simple photographs of emission color are sufficiently distinct to allow the discrimination among structurally closely related analytes, especially if the photographs are taken in different solvents or using more than one cruciform sensor. Using this quick methodology, dozens of analytes can be quickly analyzed in an afternoon (see panels in Figures 3-5), whereas the same analysis would require weeks if rigorous spectroscopy was employed. Furthermore, since boronic acids are dynamic species that can coordinate nucleophiles through boron&#39;s empty p-orbital, Miljani&#263; used this feature to develop hybrid sensors composed of benzobisoxazole cruciform 4 and simple non-fluorescent boronic acid additives B1 and B5 (Figure 4).11,12 This methodology operates as follows: cruciform 4 and boronic acids complex into a transient complex 4&#183;nB1 (or 4&#183;nB5); the precise structure of this complex is at present unknown, but its fluorescence differs from that of the pure cruciform. If this solution is exposed to Lewis basic analytes, they can replace one or both -OH groups on the boronic acid,13 thus significantly altering the electronic properties of boron and, in turn, the fluorescence of the entire complex. Using this &#34;vicarious sensing&#34; methodology, sensing of phenols, organic amines and ureas, as well as of small organic and inorganic anions, could be achieved.
In this paper, we present a tutorial on the use of both direct and vicarious sensing methodology to quickly qualitatively distinguish between structurally related (a) carboxylic acids (Figure 3), (b) boronic acids (Figure 4), and, vicariously, (c) organic amines (Figure 5). To illustrate the broad applicability of the reported protocols, Bunz&#39;s cruciforms were used to detect carboxylic acids, while Miljani&#263;&#39;s compounds were employed to detect boronic acids, and, through a hybrid sensor, small organic amines. We presume that these sensors could be readily interchanged without major consequences to the quality of analyte discrimination.

<table border="1">
		<tbody>
		 <tr>
			<td>Name of Material/ Equipment</td>
			<td>Company</td>
			<td>Catalog Number</td>
			<td>Comments/Description</td>
		 </tr>
		 <tr>
			<td>Cyclohexane (CH)</td>
			<td>Mallinckrodt</td>
			<td>4878-02</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Chlorobenzene (CB)</td>
			<td>JT Baker</td>
			<td>9179-1</td>
			<td></td>
		 </tr>
		 <tr>
			<td>1,2,4-Trichlorobenzene (TCB)</td>
			<td>Alfa Aesar</td>
			<td>19390</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Dichloromethane (DCM) - Miljani&#263;</td>
			<td>Mallinckrodt</td>
			<td>4879-06</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Acetonitrile (AN)</td>
			<td>Mallinckrodt</td>
			<td>2856-10</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Chloroform (CF)</td>
			<td>Mallinckrodt</td>
			<td>4440-19</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Dichloromethane (DCM) - Bunz</td>
			<td>Sigma Aldrich</td>
			<td>24233</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Ethyl Acetate (EtOAc)</td>
			<td>Brenntag</td>
			<td>10010447</td>
			<td>Additional distillation</td>
		 </tr>
		 <tr>
			<td>Acetonitrile (AN)</td>
			<td>Sigma Aldrich</td>
			<td>34851</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Dimethylformamide (DMF)</td>
			<td>Sigma Aldrich</td>
			<td>38840</td>
			<td></td>
		 </tr>
		 <tr>
			<td>2-Propanol (iPrOH)</td>
			<td>Ruprecht-Karls Universit&auml;t Heidelberg, Zentralbereich Neuenheimer Feld</td>
			<td>69595</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Methanol (MeOH)</td>
			<td>VWR</td>
			<td>20847.295</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Hydroxybenzoic Acid (A1)</td>
			<td>Fluka</td>
			<td>54630</td>
			<td></td>
		 </tr>
		 <tr>
			<td>(4-Hydroxyphenyl)acetic Acid (A2)</td>
			<td>Sigma Aldrich</td>
			<td>H50004</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Ibuprofen (A3)</td>
			<td>ABCR</td>
			<td>AB125950</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Aspirine (A4)</td>
			<td>Sigma Aldrich</td>
			<td>A5376</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Phenylacetic Acid (A5)</td>
			<td>Sigma Aldrich</td>
			<td>P16621</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Chlorophenylacetic Acid (A6)</td>
			<td>Sigma Aldrich</td>
			<td>139262</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Benzoic Acid (A7)</td>
			<td>Merck</td>
			<td>8222571000</td>
			<td></td>
		 </tr>
		 <tr>
			<td>3,5-Dihydroxybenzoic Acid (A8)</td>
			<td>Sigma Aldrich</td>
			<td>D110000</td>
			<td></td>
		 </tr>
		 <tr>
			<td>2,4-Dichlorobenzoic Acid (A9)</td>
			<td>Sigma Aldrich</td>
			<td>139572</td>
			<td></td>
		 </tr>
		 <tr>
			<td>2-Hydroxy-5-iodobenzoic Acid (A10)</td>
			<td>Sigma Aldrich</td>
			<td>I10600</td>
			<td></td>
		 </tr>
		 <tr>
			<td>2,6-Dichlorophenylboronic Acid (B1)</td>
			<td>TCI</td>
			<td>D3357</td>
			<td></td>
		 </tr>
		 <tr>
			<td>3,5-Bis(trifluoromethyl)phenylboronic Acid (B2)</td>
			<td>Sigma Aldrich</td>
			<td>471070</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Mercaptophenylboronic Acid (B3)</td>
			<td>Sigma Aldrich</td>
			<td>524018</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Methoxyphenylboronic Acid (B4)</td>
			<td>TCI</td>
			<td>M1126</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Benzeneboronic Acid (B5)</td>
			<td>Alfa Aesar</td>
			<td>A14257</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Cyclohexylboronic Acid (B6)</td>
			<td>Sigma Aldrich</td>
			<td>556580</td>
			<td></td>
		 </tr>
		 <tr>
			<td>3-Pyridylboronic Acid (B7)</td>
			<td>Sigma Aldrich</td>
			<td>512125</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Nitrophenylboronic Acid (B8)</td>
			<td>Sigma Aldrich</td>
			<td>673854</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Pentafluorophenylboronic Acid (B9)</td>
			<td>Sigma Aldrich</td>
			<td>465097</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Triethylamine (N1)</td>
			<td>Alfa Aesar</td>
			<td>A12646</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Piperidine (N2)</td>
			<td>JT Baker</td>
			<td>2895-05</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Piperazine (N3)</td>
			<td>Aldrich</td>
			<td>P45907</td>
			<td></td>
		 </tr>
		 <tr>
			<td>1,4-Diaminobenzene (N4)</td>
			<td>Alfa Aesar</td>
			<td>A15680</td>
			<td></td>
		 </tr>
		 <tr>
			<td>1,3-Diaminobenzene (N5)</td>
			<td>Eastman</td>
			<td></td>
			<td></td>
		 </tr>
		 <tr>
			<td>1,2-Diaminobenzene (N6)</td>
			<td>TCI</td>
			<td>P0168</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Methoxyaniline (N7)</td>
			<td>Alfa Aesar</td>
			<td>A10946</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Aniline (N8)</td>
			<td>Acros</td>
			<td>22173-2500</td>
			<td></td>
		 </tr>
		 <tr>
			<td>4-Nitroaniline (N9)</td>
			<td>Alfa Aesar</td>
			<td>A10369</td>
			<td></td>
		 </tr>
		 <tr>
			<td>N,N-Diphenylurea (N10)</td>
			<td>Alfa Aesar</td>
			<td>A18720</td>
			<td></td>
		 </tr>
		 <tr>
			<td>N,N-Dimethylurea (N11)</td>
			<td>Alfa Aesar</td>
			<td>B21329</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Urea (N12)</td>
			<td>Mallinckrodt</td>
			<td>8648-04</td>
			<td></td>
		 </tr>
		 <tr>
			<td>Canon EOS 30D (objective EFS 18-55 mm zoom lens)</td>
			<td>Canon</td>
			<td></td>
			<td></td>
		 </tr>
		 <tr>
			<td>Canon EOS Rebel T3i (objective EFS 18-55 mm zoom lens)</td>
			<td>Canon</td>
			<td></td>
			<td></td>
		 </tr>
		 <tr>
			<td>FujiFilm FinePix S9000</td>
			<td>Fuji</td>
			<td></td>
			<td></td>
		 </tr>
		</tbody>
 </table>

qualitative identification of carboxylic acids, boronic acids, and amines using cruciform fluorophores

Molecular cruciforms are X-shaped systems in which two conjugation axes intersect at a central core. If one axis of these molecules is substituted with electron-donors, and the other with electron-acceptors, cruciforms&#39; HOMO will localize along the electron-rich and LUMO along the electron-poor axis. This spatial isolation of cruciforms&#39; frontier molecular orbitals (FMOs) is essential to their use as sensors, since analyte binding to the cruciform invariably changes its HOMO-LUMO gap and the associated optical properties. Using this principle, Bunz and Miljani&#263; groups developed 1,4-distyryl-2,5-bis(arylethynyl)benzene and benzobisoxazole cruciforms, respectively, which act as fluorescent sensors for metal ions, carboxylic acids, boronic acids, phenols, amines, and anions. The emission colors observed when these cruciform are mixed with analytes are highly sensitive to the details of analyte&#39;s structure and - because of cruciforms&#39; charge-separated excited states - to the solvent in which emission is observed. Structurally closely related species can be qualitatively distinguished within several analyte classes: (a) carboxylic acids; (b) boronic acids, and (c) metals. Using a hybrid sensing system composed from benzobisoxazole cruciforms and boronic acid additives, we were also able to discern among structurally similar: (d) small organic and inorganic anions, (e) amines, and (f) phenols. The method used for this qualitative distinction is exceedingly simple. Dilute solutions (typically 10-6 M) of cruciforms in several off-the-shelf solvents are placed in UV/Vis vials. Then, analytes of interest are added, either directly as solids or in concentrated solution. Fluorescence changes occur virtually instantaneously and can be recorded through standard digital photography using a semi-professional digital camera in a dark room. With minimal graphic manipulation, representative cut-outs of emission color photographs can be arranged into panels which permit quick naked-eye distinction among analytes. For quantification purposes, Red/Green/Blue values can be extracted from these photographs and the obtained numeric data can be statistically processed.

To illustrate the potential of cruciform fluorophores in sensing and discriminating closely related analytes, three classes of results are presented. First, 1,4-distyryl-2,5-bis(arylethynyl)benzene cruciforms 1-3 (Figure 1) are used to discriminate among structurally related carboxylic acids A1-A10 shown in Figure 3. Then, benzobisoxazole-based cruciform 4 (Figure 1) has been used to analyze boronic acids B1-B9 (Figure 4). Finally, cruciform 4 is used in...

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Qualitative Identification of Carboxylic Acids, Boronic Acids, and Amines Using Cruciform Fluorophores

Cross-conjugated cruciform fluorophores based on 1,4-distyryl-2,5-bis(arylethynyl)benzene and benzobisoxazole nuclei can be used to qualitatively identify diverse Lewis acidic and Lewis basic analytes. This method relies on the differences in emission colors of the cruciforms that are observed upon analyte addition. Structurally closely related species can be distinguished from each other.

Molecular cruciforms are X-shaped systems in which two conjugation axes intersect at a central core. If one axis of these molecules is substituted with ...

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15.4K Views.  Ruprecht-Karls-Universität Heidelberg. Cross-conjugated cruciform fluorophores based on 1,4-distyryl-2,5-bis(arylethynyl)benzene and benzobisoxazole nuclei can be used to qualitatively identify diverse Lewis acidic and Lewis basic analytes. This method relies on the differences in emission colors of the cruciforms that are observed upon analyte addition. Structurally closely related species can be distinguished from each other.