Luminescent Fluorene-Based Bis-Pyrazolyl Aniline Ligand for Aluminum Detection View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2013-09-29

AUTHORS

Andrew Frazer, Alma R. Morales, Adam W. Woodward, Paul Tongwa, Tatiana Timofeeva, Kevin D. Belfield

ABSTRACT

The design, synthesis, and photophysical properties of a new fluorene-based fluorescent chemosensor, 4-((E)-2-(2-(benzo[d]thiazol-2-yl)-9,9-diethyl-9H-fluoren-7-yl)vinyl)-N,N-bis((3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzenamine (AXF-Al), is described for the detection of Al3+. AXF-Al exhibited absorption at 382 nm and strong fluorescence emission at 542 nm (fluorescence quantum yield, ΦF, of 0.80). The capture of Al3+ by the pyrazolyl aniline receptor resulted in nominal change in the linear absorption (372 nm) but a large hypsochromic shift of 161 nm in the fluorescence spectrum (542 to 433 nm, ΦF = 0.88), from which Al3+ was detected both ratiometrically and colorimetrically. The addition of other metal ions, namely Mg2+, Ca2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg 2+ and Pb2+, produced only minimal changes in the optical properties of this probe. The emission band of this probe was also accessed by two-photon excitation in the near-IR, as two-photon absorption (2PA) is important for potential applications in two-photon fluorescence microscopy (2PFM) imaging. The 2PA cross section of the free fluorenyl ligand AXF-Al was 220 GM at 810 nm and 235 GM at 810 nm for the Al-ligand complex, practically useful properties for 2PFM. More... »

PAGES

239-250

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10895-013-1291-x

DOI

http://dx.doi.org/10.1007/s10895-013-1291-x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1024229388

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/24078297


Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
Incoming Citations Browse incoming citations for this publication using opencitations.net

JSON-LD is the canonical representation for SciGraph data.

TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

[
  {
    "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
    "about": [
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Chemical Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0301", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Analytical Chemistry", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0306", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Physical Chemistry (incl. Structural)", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA", 
          "id": "http://www.grid.ac/institutes/grid.170430.1", 
          "name": [
            "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Frazer", 
        "givenName": "Andrew", 
        "id": "sg:person.0637277134.57", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0637277134.57"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA", 
          "id": "http://www.grid.ac/institutes/grid.170430.1", 
          "name": [
            "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Morales", 
        "givenName": "Alma R.", 
        "id": "sg:person.01325137217.89", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01325137217.89"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA", 
          "id": "http://www.grid.ac/institutes/grid.170430.1", 
          "name": [
            "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Woodward", 
        "givenName": "Adam W.", 
        "id": "sg:person.0705412334.57", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0705412334.57"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Department of Biology and Chemistry, New Mexico Highlands University, 87701, Las Vegas, NM, USA", 
          "id": "http://www.grid.ac/institutes/grid.260899.c", 
          "name": [
            "Department of Biology and Chemistry, New Mexico Highlands University, 87701, Las Vegas, NM, USA"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Tongwa", 
        "givenName": "Paul", 
        "id": "sg:person.01156110714.05", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01156110714.05"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Department of Biology and Chemistry, New Mexico Highlands University, 87701, Las Vegas, NM, USA", 
          "id": "http://www.grid.ac/institutes/grid.260899.c", 
          "name": [
            "Department of Biology and Chemistry, New Mexico Highlands University, 87701, Las Vegas, NM, USA"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Timofeeva", 
        "givenName": "Tatiana", 
        "id": "sg:person.01076241056.01", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01076241056.01"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "CREOL, The College of Optics and Photonics, University of Central Florida, 32816-2366, Orlando, FL, USA", 
          "id": "http://www.grid.ac/institutes/grid.170430.1", 
          "name": [
            "Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA", 
            "CREOL, The College of Optics and Photonics, University of Central Florida, 32816-2366, Orlando, FL, USA"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Belfield", 
        "givenName": "Kevin D.", 
        "id": "sg:person.01077620542.97", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01077620542.97"
        ], 
        "type": "Person"
      }
    ], 
    "citation": [
      {
        "id": "sg:pub.10.1007/s00198-005-1981-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1021770443", 
          "https://doi.org/10.1007/s00198-005-1981-6"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1023/a:1021322228428", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1020071762", 
          "https://doi.org/10.1023/a:1021322228428"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/s00204-008-0345-3", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1050366374", 
          "https://doi.org/10.1007/s00204-008-0345-3"
        ], 
        "type": "CreativeWork"
      }, 
      {
        "id": "sg:pub.10.1007/978-1-4757-3061-6", 
        "sameAs": [
          "https://app.dimensions.ai/details/publication/pub.1034475674", 
          "https://doi.org/10.1007/978-1-4757-3061-6"
        ], 
        "type": "CreativeWork"
      }
    ], 
    "datePublished": "2013-09-29", 
    "datePublishedReg": "2013-09-29", 
    "description": "The design, synthesis, and photophysical properties of a new fluorene-based fluorescent chemosensor, 4-((E)-2-(2-(benzo[d]thiazol-2-yl)-9,9-diethyl-9H-fluoren-7-yl)vinyl)-N,N-bis((3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzenamine (AXF-Al), is described for the detection of Al3+. AXF-Al exhibited absorption at 382\u00a0nm and strong fluorescence emission at 542\u00a0nm (fluorescence quantum yield, \u03a6F, of 0.80). The capture of Al3+ by the pyrazolyl aniline receptor resulted in nominal change in the linear absorption (372\u00a0nm) but a large hypsochromic shift of 161\u00a0nm in the fluorescence spectrum (542 to 433\u00a0nm, \u03a6F\u2009=\u20090.88), from which Al3+ was detected both ratiometrically and colorimetrically. The addition of other metal ions, namely Mg2+, Ca2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg 2+ and Pb2+, produced only minimal changes in the optical properties of this probe. The emission band of this probe was also accessed by two-photon excitation in the near-IR, as two-photon absorption (2PA) is important for potential applications in two-photon fluorescence microscopy (2PFM) imaging. The 2PA cross section of the free fluorenyl ligand AXF-Al was 220\u00a0GM at 810\u00a0nm and 235\u00a0GM at 810\u00a0nm for the Al-ligand complex, practically useful properties for 2PFM.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/s10895-013-1291-x", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isFundedItemOf": [
      {
        "id": "sg:grant.3106094", 
        "type": "MonetaryGrant"
      }, 
      {
        "id": "sg:grant.3093046", 
        "type": "MonetaryGrant"
      }, 
      {
        "id": "sg:grant.3094671", 
        "type": "MonetaryGrant"
      }
    ], 
    "isPartOf": [
      {
        "id": "sg:journal.1101956", 
        "issn": [
          "1053-0509", 
          "1573-4994"
        ], 
        "name": "Journal of Fluorescence", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "1", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "24"
      }
    ], 
    "keywords": [
      "detection of Al3", 
      "large hypsochromic shift", 
      "strong fluorescence emission", 
      "Al-ligand complex", 
      "aniline ligands", 
      "photophysical properties", 
      "fluorescent chemosensor", 
      "metal ions", 
      "Hg 2", 
      "hypsochromic shift", 
      "fluorescence emission", 
      "aluminum detection", 
      "fluorescence spectra", 
      "two-photon absorption", 
      "optical properties", 
      "emission band", 
      "Al3", 
      "potential applications", 
      "two-photon excitation", 
      "linear absorption", 
      "two-photon fluorescence microscopy", 
      "useful properties", 
      "absorption", 
      "properties", 
      "chemosensor", 
      "Cu2", 
      "fluorescence microscopy", 
      "IR", 
      "Ni2", 
      "fluorene", 
      "Pb2", 
      "ligands", 
      "probe", 
      "ions", 
      "Zn2", 
      "synthesis", 
      "Fe2", 
      "complexes", 
      "nominal changes", 
      "Cd2", 
      "Mn2", 
      "microscopy", 
      "CO2", 
      "spectra", 
      "detection", 
      "Mg2", 
      "emission", 
      "band", 
      "capture", 
      "excitation", 
      "shift", 
      "applications", 
      "cross sections", 
      "addition", 
      "minimal changes", 
      "Ca2", 
      "changes", 
      "design", 
      "GM", 
      "sections", 
      "receptors", 
      "new fluorene-based fluorescent chemosensor", 
      "fluorene-based fluorescent chemosensor", 
      "AXF-Al", 
      "capture of Al3", 
      "pyrazolyl aniline receptor", 
      "aniline receptor", 
      "free fluorenyl ligand AXF-Al", 
      "fluorenyl ligand AXF-Al", 
      "ligand AXF-Al", 
      "Luminescent Fluorene", 
      "Bis-Pyrazolyl Aniline Ligand"
    ], 
    "name": "Luminescent Fluorene-Based Bis-Pyrazolyl Aniline Ligand for Aluminum Detection", 
    "pagination": "239-250", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1024229388"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/s10895-013-1291-x"
        ]
      }, 
      {
        "name": "pubmed_id", 
        "type": "PropertyValue", 
        "value": [
          "24078297"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/s10895-013-1291-x", 
      "https://app.dimensions.ai/details/publication/pub.1024229388"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2021-12-01T19:30", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20211201/entities/gbq_results/article/article_607.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/s10895-013-1291-x"
  }
]
 

Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/s10895-013-1291-x'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/s10895-013-1291-x'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/s10895-013-1291-x'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/s10895-013-1291-x'


 

This table displays all metadata directly associated to this object as RDF triples.

200 TRIPLES      22 PREDICATES      103 URIs      90 LITERALS      7 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/s10895-013-1291-x schema:about anzsrc-for:03
2 anzsrc-for:0301
3 anzsrc-for:0306
4 schema:author N39dcc8b8595146f0a0b6a253e3a9c15d
5 schema:citation sg:pub.10.1007/978-1-4757-3061-6
6 sg:pub.10.1007/s00198-005-1981-6
7 sg:pub.10.1007/s00204-008-0345-3
8 sg:pub.10.1023/a:1021322228428
9 schema:datePublished 2013-09-29
10 schema:datePublishedReg 2013-09-29
11 schema:description The design, synthesis, and photophysical properties of a new fluorene-based fluorescent chemosensor, 4-((E)-2-(2-(benzo[d]thiazol-2-yl)-9,9-diethyl-9H-fluoren-7-yl)vinyl)-N,N-bis((3,5-dimethyl-1H-pyrazol-1-yl)methyl)benzenamine (AXF-Al), is described for the detection of Al3+. AXF-Al exhibited absorption at 382 nm and strong fluorescence emission at 542 nm (fluorescence quantum yield, ΦF, of 0.80). The capture of Al3+ by the pyrazolyl aniline receptor resulted in nominal change in the linear absorption (372 nm) but a large hypsochromic shift of 161 nm in the fluorescence spectrum (542 to 433 nm, ΦF = 0.88), from which Al3+ was detected both ratiometrically and colorimetrically. The addition of other metal ions, namely Mg2+, Ca2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, Hg 2+ and Pb2+, produced only minimal changes in the optical properties of this probe. The emission band of this probe was also accessed by two-photon excitation in the near-IR, as two-photon absorption (2PA) is important for potential applications in two-photon fluorescence microscopy (2PFM) imaging. The 2PA cross section of the free fluorenyl ligand AXF-Al was 220 GM at 810 nm and 235 GM at 810 nm for the Al-ligand complex, practically useful properties for 2PFM.
12 schema:genre article
13 schema:inLanguage en
14 schema:isAccessibleForFree false
15 schema:isPartOf N168c297b92d6489090d342d23e537814
16 N735f8ed90d3549c684471673402be627
17 sg:journal.1101956
18 schema:keywords AXF-Al
19 Al-ligand complex
20 Al3
21 Bis-Pyrazolyl Aniline Ligand
22 CO2
23 Ca2
24 Cd2
25 Cu2
26 Fe2
27 GM
28 Hg 2
29 IR
30 Luminescent Fluorene
31 Mg2
32 Mn2
33 Ni2
34 Pb2
35 Zn2
36 absorption
37 addition
38 aluminum detection
39 aniline ligands
40 aniline receptor
41 applications
42 band
43 capture
44 capture of Al3
45 changes
46 chemosensor
47 complexes
48 cross sections
49 design
50 detection
51 detection of Al3
52 emission
53 emission band
54 excitation
55 fluorene
56 fluorene-based fluorescent chemosensor
57 fluorenyl ligand AXF-Al
58 fluorescence emission
59 fluorescence microscopy
60 fluorescence spectra
61 fluorescent chemosensor
62 free fluorenyl ligand AXF-Al
63 hypsochromic shift
64 ions
65 large hypsochromic shift
66 ligand AXF-Al
67 ligands
68 linear absorption
69 metal ions
70 microscopy
71 minimal changes
72 new fluorene-based fluorescent chemosensor
73 nominal changes
74 optical properties
75 photophysical properties
76 potential applications
77 probe
78 properties
79 pyrazolyl aniline receptor
80 receptors
81 sections
82 shift
83 spectra
84 strong fluorescence emission
85 synthesis
86 two-photon absorption
87 two-photon excitation
88 two-photon fluorescence microscopy
89 useful properties
90 schema:name Luminescent Fluorene-Based Bis-Pyrazolyl Aniline Ligand for Aluminum Detection
91 schema:pagination 239-250
92 schema:productId N1b3ac80828d0411bb6e54d3d1f642716
93 N2212bbfa0a2e4169bdecde19e02e9dc0
94 Nad6b5d2be45c46efb46bb55f42e702f1
95 schema:sameAs https://app.dimensions.ai/details/publication/pub.1024229388
96 https://doi.org/10.1007/s10895-013-1291-x
97 schema:sdDatePublished 2021-12-01T19:30
98 schema:sdLicense https://scigraph.springernature.com/explorer/license/
99 schema:sdPublisher N813f3d8eb18a4924b0bd084a750d0c63
100 schema:url https://doi.org/10.1007/s10895-013-1291-x
101 sgo:license sg:explorer/license/
102 sgo:sdDataset articles
103 rdf:type schema:ScholarlyArticle
104 N04b6b7b5b1ab449d97219c5677e38f0b rdf:first sg:person.0705412334.57
105 rdf:rest N10781376077b45cea0d30265fc511bd7
106 N10781376077b45cea0d30265fc511bd7 rdf:first sg:person.01156110714.05
107 rdf:rest Nde967a8706d54fccbe78dc7f93ea5362
108 N168c297b92d6489090d342d23e537814 schema:volumeNumber 24
109 rdf:type schema:PublicationVolume
110 N1b3ac80828d0411bb6e54d3d1f642716 schema:name dimensions_id
111 schema:value pub.1024229388
112 rdf:type schema:PropertyValue
113 N2212bbfa0a2e4169bdecde19e02e9dc0 schema:name pubmed_id
114 schema:value 24078297
115 rdf:type schema:PropertyValue
116 N39dcc8b8595146f0a0b6a253e3a9c15d rdf:first sg:person.0637277134.57
117 rdf:rest Nc873809e79c2433b894e71aaa850f6e7
118 N735f8ed90d3549c684471673402be627 schema:issueNumber 1
119 rdf:type schema:PublicationIssue
120 N76cf628234474d2196777ada18d4e1b1 rdf:first sg:person.01077620542.97
121 rdf:rest rdf:nil
122 N813f3d8eb18a4924b0bd084a750d0c63 schema:name Springer Nature - SN SciGraph project
123 rdf:type schema:Organization
124 Nad6b5d2be45c46efb46bb55f42e702f1 schema:name doi
125 schema:value 10.1007/s10895-013-1291-x
126 rdf:type schema:PropertyValue
127 Nc873809e79c2433b894e71aaa850f6e7 rdf:first sg:person.01325137217.89
128 rdf:rest N04b6b7b5b1ab449d97219c5677e38f0b
129 Nde967a8706d54fccbe78dc7f93ea5362 rdf:first sg:person.01076241056.01
130 rdf:rest N76cf628234474d2196777ada18d4e1b1
131 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
132 schema:name Chemical Sciences
133 rdf:type schema:DefinedTerm
134 anzsrc-for:0301 schema:inDefinedTermSet anzsrc-for:
135 schema:name Analytical Chemistry
136 rdf:type schema:DefinedTerm
137 anzsrc-for:0306 schema:inDefinedTermSet anzsrc-for:
138 schema:name Physical Chemistry (incl. Structural)
139 rdf:type schema:DefinedTerm
140 sg:grant.3093046 http://pending.schema.org/fundedItem sg:pub.10.1007/s10895-013-1291-x
141 rdf:type schema:MonetaryGrant
142 sg:grant.3094671 http://pending.schema.org/fundedItem sg:pub.10.1007/s10895-013-1291-x
143 rdf:type schema:MonetaryGrant
144 sg:grant.3106094 http://pending.schema.org/fundedItem sg:pub.10.1007/s10895-013-1291-x
145 rdf:type schema:MonetaryGrant
146 sg:journal.1101956 schema:issn 1053-0509
147 1573-4994
148 schema:name Journal of Fluorescence
149 schema:publisher Springer Nature
150 rdf:type schema:Periodical
151 sg:person.01076241056.01 schema:affiliation grid-institutes:grid.260899.c
152 schema:familyName Timofeeva
153 schema:givenName Tatiana
154 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01076241056.01
155 rdf:type schema:Person
156 sg:person.01077620542.97 schema:affiliation grid-institutes:grid.170430.1
157 schema:familyName Belfield
158 schema:givenName Kevin D.
159 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01077620542.97
160 rdf:type schema:Person
161 sg:person.01156110714.05 schema:affiliation grid-institutes:grid.260899.c
162 schema:familyName Tongwa
163 schema:givenName Paul
164 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01156110714.05
165 rdf:type schema:Person
166 sg:person.01325137217.89 schema:affiliation grid-institutes:grid.170430.1
167 schema:familyName Morales
168 schema:givenName Alma R.
169 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01325137217.89
170 rdf:type schema:Person
171 sg:person.0637277134.57 schema:affiliation grid-institutes:grid.170430.1
172 schema:familyName Frazer
173 schema:givenName Andrew
174 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0637277134.57
175 rdf:type schema:Person
176 sg:person.0705412334.57 schema:affiliation grid-institutes:grid.170430.1
177 schema:familyName Woodward
178 schema:givenName Adam W.
179 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.0705412334.57
180 rdf:type schema:Person
181 sg:pub.10.1007/978-1-4757-3061-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1034475674
182 https://doi.org/10.1007/978-1-4757-3061-6
183 rdf:type schema:CreativeWork
184 sg:pub.10.1007/s00198-005-1981-6 schema:sameAs https://app.dimensions.ai/details/publication/pub.1021770443
185 https://doi.org/10.1007/s00198-005-1981-6
186 rdf:type schema:CreativeWork
187 sg:pub.10.1007/s00204-008-0345-3 schema:sameAs https://app.dimensions.ai/details/publication/pub.1050366374
188 https://doi.org/10.1007/s00204-008-0345-3
189 rdf:type schema:CreativeWork
190 sg:pub.10.1023/a:1021322228428 schema:sameAs https://app.dimensions.ai/details/publication/pub.1020071762
191 https://doi.org/10.1023/a:1021322228428
192 rdf:type schema:CreativeWork
193 grid-institutes:grid.170430.1 schema:alternateName CREOL, The College of Optics and Photonics, University of Central Florida, 32816-2366, Orlando, FL, USA
194 Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA
195 schema:name CREOL, The College of Optics and Photonics, University of Central Florida, 32816-2366, Orlando, FL, USA
196 Department of Chemistry, University of Central Florida, 32816-2366, Orlando, FL, USA
197 rdf:type schema:Organization
198 grid-institutes:grid.260899.c schema:alternateName Department of Biology and Chemistry, New Mexico Highlands University, 87701, Las Vegas, NM, USA
199 schema:name Department of Biology and Chemistry, New Mexico Highlands University, 87701, Las Vegas, NM, USA
200 rdf:type schema:Organization
 




Preview window. Press ESC to close (or click here)


...