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2.4 to 3.4 GHz

Design and Characterization of a 5 2 GHz/2 4 GHz Fractional  Frequency Synthesizer for Low Phase Noise Performance

Design and Characterization of a 5 2 GHz/2 4 GHz Fractional Frequency Synthesizer for Low Phase Noise Performance

... the ΣΔ modulator. The ΣΔ noise shaping can be modeled as a linear gain stage with an additive quantization noise source, which is shaped by a highpass transfer function. Hence, the quantization error component at the ...

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A Survey on Interference Mitigation Techniques for 2 4 GHz ISM Band

A Survey on Interference Mitigation Techniques for 2 4 GHz ISM Band

... technique to mitigate interference in the environment. From various study, it is found that usage of common spectrum suffers from interference and effective interference mitigation mechanism is needed for the ...

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MIMO Reconfigurable Antennas for Wi Fi 2 4 GHz Communication

MIMO Reconfigurable Antennas for Wi Fi 2 4 GHz Communication

... The most common and frequent use of local wireless communication is Wi-Fi technology for the purpose of accessing any type of document, audio, video from Internet through smartphones, tablets or laptops. From 2018 to ...

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QuickSpecs. At A Glance. HP Integrity rx Server. Overview

QuickSpecs. At A Glance. HP Integrity rx Server. Overview

... A9738A–Supports from 4 to 16 DIMMs (1- to 64-GB); 12.8 GB/s memory bandwidth A9739A–Supports from 4 to 32 DIMMs (1- to 128-GB); 12.8 GB/s memory bandwidth Both memory carrier boards provide the same ...

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N [4 Cyano 3 (tri­fluoro­meth­yl)phen­yl] 3 (4 fluoro­phenyl­sulfon­yl) 2 hydr­­oxy 2 methyl­propionamide

N [4 Cyano 3 (tri­fluoro­meth­yl)phen­yl] 3 (4 fluoro­phenyl­sulfon­yl) 2 hydr­­oxy 2 methyl­propionamide

... Sheldrick, G. M. (1997). SHELXS97. University of Go¨ttingen, Germany. Sepp-Lorenzino, L. & Slovin, S. (2000). Expert Opin. Ther. Pat. 10, 1833–1842. Tetsuya, S., Tadashi, K. & Nobushige, I. (2003). US Patent 2003 ...

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2 (Biphen­yl 4 yl) 3 (4 meth­oxy­phen­yl) 1,3 thia­zolidin 4 one

2 (Biphen­yl 4 yl) 3 (4 meth­oxy­phen­yl) 1,3 thia­zolidin 4 one

... 4-Methoxyaniline (5 g, 1 mol), 4-biphenylcarboxaldehyde (7.39 g, 1.0 mol) and anhydrous -ferrite (12.96 g, 2 mol) were refluxed with constant stirring in dry benzene for 30 min, after which ...

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3 (2 Amino­ethyl) 2 (4 fluoroanilino)­quinazolin 4(3H) one

3 (2 Amino­ethyl) 2 (4 fluoroanilino)­quinazolin 4(3H) one

... of 2-ethoxycarbonyliminophosphorane (1.27 g, 3 mmol) in 10 ml anhydrous THF, 4-chlorophenyliso- cyanate ...g, 3 mmol) was added dropwise at room ...g, 3 mmol) in 5 ml anhydrous ...CH ...

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2 (4 Fluoro­anilino) 3 (2 hy­droxy­ethyl)quinazolin 4(3H) one

2 (4 Fluoro­anilino) 3 (2 hy­droxy­ethyl)quinazolin 4(3H) one

... C15 0.0535 (7) 0.0494 (7) 0.0348 (6) 0.0053 (6) 0.0160 (5) −0.0031 (5) C16 0.0621 (8) 0.0616 (8) 0.0327 (6) 0.0034 (6) 0.0092 (6) −0.0009 (6) F1 0.0736 (6) 0.0599 (5) 0.0592 (5) −0.0229 (4) 0.0116 (4) ...

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3 Eth­­oxy 4 [2 (2 eth­oxy 4 formyl­phen­­oxy)eth­­oxy]benzaldehyde

3 Eth­­oxy 4 [2 (2 eth­oxy 4 formyl­phen­­oxy)eth­­oxy]benzaldehyde

... C6 0.0379 (8) 0.0383 (8) 0.0399 (8) −0.0016 (6) 0.0088 (6) 0.0033 (6) C7 0.0373 (8) 0.0359 (8) 0.0446 (8) −0.0070 (6) 0.0100 (6) 0.0067 (6) C8 0.0610 (12) 0.0725 (13) 0.0546 (11) 0.0148 (10) 0.0195 (9) −0.0044 (10) C9 ...

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4 [2 (4 Fluoro­phen­yl)furan 3 yl]pyridine

4 [2 (4 Fluoro­phen­yl)furan 3 yl]pyridine

... The analysis of the crystal structure of the title compound is shown in Fig. 1. The furan ring makes dihedral angles of 40.04 (11)° and 25.71 (11)° to the pyridine ring and the 4-fluorophenyl ring, respectively. ...

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2 (4 Chloro­phenyl) 3 cyclo­hexyl­thia­zolidin 4 one1 1

2 (4 Chloro­phenyl) 3 cyclo­hexyl­thia­zolidin 4 one1 1

... S1 0.0430 (4) 0.0896 (6) 0.0808 (5) 0.0129 (4) 0.0002 (3) −0.0059 (5) C2 0.0405 (13) 0.0515 (16) 0.0565 (15) 0.0016 (12) 0.0073 (11) 0.0039 (13) N3 0.0439 (11) 0.0568 (13) 0.0463 (12) 0.0012 (11) ...

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Methyl 2 benzyl 5 [1 (4 meth­oxy­phen­yl) 4 oxo 3 phenyl­azetidin 2 yl] 4 nitro 3 phenyl­pyrrolidine 2 carboxyl­ate

Methyl 2 benzyl 5 [1 (4 meth­oxy­phen­yl) 4 oxo 3 phenyl­azetidin 2 yl] 4 nitro 3 phenyl­pyrrolidine 2 carboxyl­ate

... C34 0.0576 (11) 0.0546 (10) 0.0370 (9) 0.0031 (8) 0.0038 (7) 0.0007 (7) C35 0.0508 (10) 0.0430 (9) 0.0480 (9) −0.0006 (8) 0.0117 (8) −0.0037 (7) C36 0.0572 (11) 0.0418 (9) 0.0508 (10) 0.0072 (8) 0.0096 (8) 0.0077 (7) C37 ...

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2 [1 (4 Bromo­phen­yl) 3 hy­dr­oxy 3 (4 meth­­oxy­phen­yl)prop­yl]cyclo­hexa­nol

2 [1 (4 Bromo­phen­yl) 3 hy­dr­oxy 3 (4 meth­­oxy­phen­yl)prop­yl]cyclo­hexa­nol

... from 2-(1-(4-bromo- phenyl)-3-(4-methoxyphenyl)-3-oxopropyl)cyclohexanone (1,5-diketone) (Ceylan & Gezegen, 2008; Gezegen et ...of ...

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Crystal structure of 2 (4 chloro­phen­yl) 3 (4 meth­­oxy­phen­yl) 3 (methyl­sulfanyl)­acrylo­nitrile

Crystal structure of 2 (4 chloro­phen­yl) 3 (4 meth­­oxy­phen­yl) 3 (methyl­sulfanyl)­acrylo­nitrile

... Cl7 0.0571 (3) 0.0760 (5) 0.0789 (4) 0.0308 (3) 0.0114 (3) 0.0093 (4) S12 0.0507 (3) 0.0523 (3) 0.0385 (3) 0.0136 (2) 0.0150 (2) 0.0035 (2) O20 ...

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4′ Methyl 3 (4 nitro­phen­yl) 4 phenyl 4,5,1′,2′,3′,4′ hexa­hydro­spiro­[isoxazole 5,2′ naphthalen] 1′ one

4′ Methyl 3 (4 nitro­phen­yl) 4 phenyl 4,5,1′,2′,3′,4′ hexa­hydro­spiro­[isoxazole 5,2′ naphthalen] 1′ one

... In a 100 ml flask, 2 mmoles (0.5 g) of (I) and 0.4 g (2.4 mmoles) mmoles of (II) were dissolved in 20 ml of chloroform. The mixture was cooled to 0°C under magnetic stirring in an ice bath. Then 15 ml of bleach at ...

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4 (3 Meth­oxy­phenyl­diazen­yl) 2 methyl­phenol

4 (3 Meth­oxy­phenyl­diazen­yl) 2 methyl­phenol

... used to solve structure: SHELXS97 Sheldrick, 1997; programs used to refine structure: SHELXL97 Sheldrick, 1997; molecular graphics: ORTEP-3 for Windows Farrugia, 1997; software used to p[r] ...

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Methyl 3 (2 chloro­phenyl) 2 (1H indol 3 ylmethyl) 5 [1 (4 methoxyphenyl) 4 oxo 3 phenylazetidin 2 yl] 4 nitropyr­rolidine 2 carboxylate

Methyl 3 (2 chloro­phenyl) 2 (1H indol 3 ylmethyl) 5 [1 (4 methoxyphenyl) 4 oxo 3 phenylazetidin 2 yl] 4 nitropyr­rolidine 2 carboxylate

... C26 0.057 (2) 0.062 (3) 0.060 (2) 0.032 (2) 0.0248 (18) 0.017 (2) C27 0.059 (2) 0.064 (3) 0.085 (3) 0.044 (2) 0.032 (2) 0.027 (2) C28 0.057 ...

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3 [3 (4 Chloro­phen­yl) 4 oxo­thia­zolidin 2 yl] 6 meth­yl 4H benzo­pyran 4 one

3 [3 (4 Chloro­phen­yl) 4 oxo­thia­zolidin 2 yl] 6 meth­yl 4H benzo­pyran 4 one

... C1 0.107 (2) 0.0602 (14) 0.0852 (17) 0.0015 (13) 0.0566 (17) −0.0136 (12) C2 0.111 (2) 0.0625 (14) 0.0649 (14) −0.0052 (14) 0.0436 (15) −0.0106 (11) C3 0.0684 (13) 0.0472 (10) 0.0547 (12) −0.0082 (9) 0.0263 ...

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Ethyl 4 (4 bromo­phen­yl) 6 (4 eth­oxy­phen­yl) 2 oxo­cyclo­hex 3 ene­carboxyl­ate

Ethyl 4 (4 bromo­phen­yl) 6 (4 eth­oxy­phen­yl) 2 oxo­cyclo­hex 3 ene­carboxyl­ate

... C20 0.073 (3) 0.077 (3) 0.068 (4) 0.016 (3) 0.022 (3) −0.004 (3) C21 0.068 (3) 0.049 (2) 0.063 (3) −0.002 (2) 0.034 (3) 0.001 (2) C22 ...

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4 [3 Benzoyl 4 (4 chloro­phen­yl) 1 methyl­pyrrolidin 2 yl] 1 (4 meth­oxy­phen­yl) 3 phenyl­azetidin 2 one

4 [3 Benzoyl 4 (4 chloro­phen­yl) 1 methyl­pyrrolidin 2 yl] 1 (4 meth­oxy­phen­yl) 3 phenyl­azetidin 2 one

... A solution of cis-4-formyl-2-azetidinone (1 mmol), sarcosine (1 mmol) and chlorochalcone (1 mmol) was refluxed in toluene (15 ml) using a Dean–Stark apparatus. The completion of the reac- tion was evidenced ...

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