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[ CAS No. 10025-98-6 ] {[proInfo.proName]}

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Chemical Structure| 10025-98-6
Chemical Structure| 10025-98-6
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Product Citations

Product Citations

Luo, Shao-Xiong Lennon ; Yuan, Weize ; Xue, Mantian , et al. DOI: PubMed ID:

Abstract: Metal nanoparticles have been widely employed in chem. sensing due to their high reactivity toward various gases. The size of the metal nanoparticles often dictates their reactivity and hence their performance as chemiresistive sensors. Herein, we report that iptycene-containing poly(arylene ether)s (PAEs) have been shown to limit the growth of palladium nanoparticles (Pd NPs) and stabilize the Pd NPs dispersion. These porous PAEs also facilitate the efficient transport of analytes. Single-walled carbon nanotube (SWCNT)-based chemiresistors and graphene field-effect transistors (GFETs) using these PAE-supported small Pd NPs are sensitive, selective, and robust sensory materials for hydrogen gas under ambient conditions. Generalizable strategies including presorting SWCNTs with pentiptycene-containing poly(p-phenylene ethynylene)s (PPEs) and thermal annealing demonstrated significant improvements in the chemiresistive performance. The polymer:NP colloids produced in this study are readily synthesized and solution processable, and these methods are of general utility.

Keywords: hydrogen ; gas sensing ; palladium nanoparticles ; carbon nanomaterials ; porous polymers

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Product Details of [ 10025-98-6 ]

CAS No. :10025-98-6 MDL No. :MFCD00011373
Formula : Cl4K2Pd Boiling Point : No data available
Linear Structure Formula :- InChI Key :LGCKLDWLSVFMGL-UHFFFAOYSA-J
M.W : 326.43 Pubchem ID :61438
Synonyms :

Calculated chemistry of [ 10025-98-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : None
Num. rotatable bonds : 0
Num. H-bond acceptors : None
Num. H-bond donors : None
Molar Refractivity : 23.41
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : None
BBB permeant : None
P-gp substrate : None
CYP1A2 inhibitor : None
CYP2C19 inhibitor : None
CYP2C9 inhibitor : None
CYP2D6 inhibitor : None
CYP3A4 inhibitor : None
Log Kp (skin permeation) : None cm/s

Lipophilicity

Log Po/w (iLOGP) : None
Log Po/w (XLOGP3) : None
Log Po/w (WLOGP) : None
Log Po/w (MLOGP) : None
Log Po/w (SILICOS-IT) : None
Consensus Log Po/w : None

Druglikeness

Lipinski : None
Ghose : None
Veber : None
Egan : None
Muegge : None
Bioavailability Score : None

Water Solubility

Log S (ESOL) : None
Solubility : None mg/ml ; None mol/l
Class : None
Log S (Ali) : None
Solubility : None mg/ml ; None mol/l
Class : None
Log S (SILICOS-IT) : None
Solubility : None mg/ml ; None mol/l
Class : None

Medicinal Chemistry

PAINS : None alert
Brenk : None alert
Leadlikeness : None
Synthetic accessibility : None

Safety of [ 10025-98-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 10025-98-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 10025-98-6 ]

[ 10025-98-6 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 23945-44-0 ]
  • [ 10025-98-6 ]
  • [ 136371-42-1 ]
  • 2
  • [ 23945-44-0 ]
  • [ 10025-98-6 ]
  • Pd(2+)*2Cl(1-)*2C5H4N2O4=PdCl2(C5H4N2O4)2 [ No CAS ]
  • 5
  • [ 10025-98-6 ]
  • [ 79286-79-6 ]
  • PdCl2(C4H10N2) [ No CAS ]
  • 6
  • [ 67-56-1 ]
  • [ 10025-98-6 ]
  • [ 547-32-0 ]
  • [ 1096051-55-6 ]
  • 7
  • [ 73-70-1 ]
  • [ 10025-98-6 ]
  • [ 81521-20-2 ]
  • 8
  • [ 10025-98-6 ]
  • [ 1000340-39-5 ]
  • C14H8Br2Cl4N4Pd [ No CAS ]
YieldReaction ConditionsOperation in experiment
In ethanol; water; at 44.84℃; for 48h; General procedure: K2PdCl4 and the seven halogeno-derivatives of 7-azaindole(3Cl7AIH, 3Br7AIH, 4Cl7AIH, 4Br7AIH, 5Br7AIH, 3Br4Cl7AIH and5Br3Cl7AIH) were purchased from Sigma-Aldrich.In the syntheses of trans-[PdCl2(L)2] we followed the procedure described earlier for obtaining trans-[PdCl2(7AIH)2] [24] and trans-[PdCl2(7AI3CAH)2] [25]. A hot aqueous solution (10 cm3) of K2PdCl4(0.5 mmol) was mixed with the ethanol solution of the appropriateligand (1.0 mmol, 20 cm3) and stirred at 318 K for 48 h. The obtained pale yellow solids were filtered off,washed with ethanol andthen dried. The results of the elemental analysis are collected in Table 1S in the Supplementary Data.
  • 9
  • [ 30709-67-2 ]
  • [ 10025-98-6 ]
  • [(Pd(2-amino-5-methyl-4-phenylthiazole)2)]Cl2 [ No CAS ]
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