| ²é¿´: 303 | »Ø¸´: 1 | ||
jinweiyangгæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú fxj.i-1µÄ½á¹¹ ÒÑÓÐ1È˲ÎÓë
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 110.56,119.43,120.04,120.33,123.34,125.83 |
» ²ÂÄãϲ»¶
081700»¯Ñ§¹¤³ÌÓë¼¼Êõ Ò»Ö¾Ô¸Öк£Ñó 323 Çóµ÷¼ÁѧУ
ÒѾÓÐ12È˻ظ´
385·Ö ÉúÎïѧ£¨071000£©Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁÏר˶283Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
0703Çóµ÷¼Á383·Ö
ÒѾÓÐ5È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
26¿¼Ñе÷¼Á0710 0860
ÒѾÓÐ8È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ£¬³õÊԳɼ¨350Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
085600£¬×¨Òµ¿Î»¯¹¤ÔÀí£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÒ»¸ö¾§ÌåµÄÍØÆË½á¹¹¼°ÍØÆË·ÖÎö
ÒѾÓÐ8È˻ظ´
ÇóÖú£¬ÔõÑù²éѯ¾ßÓÐÌØ¶¨²àÁ´½á¹¹µÄ¾ÛºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖúSAPO-34¾§Ìå½á¹¹Í¼£¨ÒªÇò¹÷Ä£Ð͵ģ©
ÒѾÓÐ5È˻ظ´
ÇóÖú£ºÈçºÎ½«chemdrawÀïµÄ½á¹¹Ê½Ëõ·ÅÖÁ75%Ö±½Ó²åÈëWORDÎĵµ£¿£¿£¿
ÒѾÓÐ5È˻ظ´
p-n½á¹¹µÄI-VÌØÐÔÎÊÌâÇóÖú
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÓйØPEIµÄ½á¹¹Ê½
ÒѾÓÐ5È˻ظ´
[ÇóÖú]¹ØÓÚ¶àëĵĽṹ·ÖÎö
ÒѾÓÐ4È˻ظ´
ÇóÖúmPEG-DSPEµÄ½á¹¹Ê½
ÒѾÓÐ5È˻ظ´
ÇóÖúb-¹ÈçÞ´¼µÄ½á¹¹Ê½
ÒѾÓÐ4È˻ظ´
ÇóÖú¹¦ÄܲÄÁÏÓë½á¹¹²ÄÁϵĵÄ׼ȷ¶¨ÒåÓë·ÖÀà
ÒѾÓÐ3È˻ظ´
[ÇóÖú¡¿1Ìâ½á¹¹»¯Ñ§
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú£ºÇëÎÊethyldiaminocarbodiimide(EDC)µÄ½á¹¹
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÇóÖúPW½á¹¹ÓÅ»¯Óöµ½µÄÎÊÌâ
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÕâÊDz»ÊÇÎÞ¶¨Ðνṹ£¿ÓÐûÓз½·¨¿ÉÒԵõ½ÎÞ¶¨ÐνṹÖеÄÔªËØ×é³É
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú HgÈí¼þÖÐÔõôһ¾§Ìå½á¹¹µÄXRDÆ×ͼ£¿
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿Çå³þµÄµ°°×Öʶþ¼¶½á¹¹Í¼
ÒѾÓÐ6È˻ظ´
ÇóÖú½âÎö¾§Ìå½á¹¹µÄһЩÊý¾Ýº¬Òå
ÒѾÓÐ2È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ¸ù¾Ý½á¹¹Ê½ÕÒÌìÈ»²úÎïµÄÀàËÆ½á¹¹
ÒѾÓÐ17È˻ظ´
¡¾ÇóÖú¡¿i-PrMgCll-LiClµÄ»¯Ñ§½á¹¹ÊÇʲô£¿ÕâÖÖÊÔ¼Áͨ³£ÓÃÓÚʲô·´Ó¦£¬
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿²ËÄñÇóÖú£¬ÈçºÎÓɵ°°×ÖʵÄÒ»¼¶½á¹¹µÃµ½Èý¼¶½á¹¹£¿
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿ÇóÖúÒ»¸öÒ©ÎïµÄ¾§Ìå½á¹¹Êý¾Ý£¡
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿ZnOµÄB2ÏàµÄ¾§Ìå½á¹¹
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿Çó¡¶¾Ûõ£Ñǰ·:»¯Ñ§.½á¹¹ÓëÐÔÄܵĹØÏµ¼°²ÄÁÏ¡·
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿3 nm µÄºË¿Ç½á¹¹Ôõô֤Ã÷°¡?
ÒѾÓÐ11È˻ظ´
¡¾ÇóÖú¡¿Çó¶àÌǵĸ߼¶½á¹¹Í¼
ÒѾÓÐ16È˻ظ´
·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jinweiyang: ½ð±Ò+8, ¡ïÓаïÖú 2015-01-05 14:59:20
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jinweiyang: ½ð±Ò+8, ¡ïÓаïÖú 2015-01-05 14:59:20
|
²éѯ½á¹û£º¹²²éµ½149¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Carbazole ÏàËÆ¶È:83.3% Molecules 2001 6 668-672 Modified Methods for the Synthesis of Carbazole from Phenothiazine R. B. Miller and Steven C. Farmer Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Carbazole ÏàËÆ¶È:83.3% Molecules 2008 13 1345-1352 Ring Contracting Sulfur Extrusion from Oxidized Phenothiazine Ring Systems Steven C. Farmer and Seth H. Berg Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . carbazole ÏàËÆ¶È:83.3% Journal of Heterocyclic Chemistry 2009 46 1309-1317 Microwave-assisted Cadogan reaction for the synthesis of 2-aryl-2H-indazoles,2-aryl-1H-benzimidazoles,2-carbonylindoles,carbazole,and phenazine Evelyn Cuevas Creencia,Masahiro Kosaka,Toshikatsu Muramatsu,Masashi Kobayashi,Tomohiro Iizuka and Takaaki Horaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Carbazole ÏàËÆ¶È:83.3% Magnetic Resonance in Chemistry 2000 38 149-155 GIAO NMR calculations for carbazole and its N-methyl and N-ethyl derivatives. Comparison of theoretical and experimental 13C chemical shifts Teobald Kupka, Grazyna Pasterna, Maria Jaworska, Aglaia Karali and Photis Dais Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1H-indazole ÏàËÆ¶È:71.4% Molecules 2006 11 867-889 Synthesis and Structural Characterization of 1- and 2-Substituted Indazoles: Ester and Carboxylic Acid Derivatives F¨¢tima C. Teixeira, H¨¦l¨¨ne Ramos, In¨ºs F. Antunes, M. J. Curto, M. T. Duarte and Isabel Bento Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Bis(carbazol-1-yl)fluormethylsilan ÏàËÆ¶È:71.4% Zeitschrift f¨¹r Naturforschung B 2004 59 1045-1050 Carbazolylsilanes: Synthesis and Crystal Structures (In German) V. Liebau, M. Noltemeyer, J. Magull, and U. Klingebie Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1H-indazole ÏàËÆ¶È:71.4% Tetrahedron 2014 70 8413-8418 A general synthesis of diversely substituted indazoles and hetero-aromatic derivatives from o-halo-(het)arylaldehydes or -phenones Emmanuelle Dubost, Silvia Stiebing, Thibault Ferrary, Thomas Cailly, Fr¨¦d¨¦ric Fabis, Val¨¦rie Collot Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Carbazole ÏàËÆ¶È:66.6% Phytochemistry 1992 31 2503-2505 Carbazole alkaloids from Glycosmis pentaphylla A. Chakraborty, B.K. Chowdhury, S.S. Jash, G.K. Biswas, S.K. Bhattacharyya, P. Bhattacharyya Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 1 ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2005 42 867-875 A study of substituent effect on 1H and 13C NMR spectra of mono,di and poly substituted carbazoles Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 1a ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2004 41 161-171 A study of substituent effect on 1H and 13C nmr spectra of N-and C-substituted carbazoles Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Z-1-vinylpyrrole-2-carbaldehyde oxime ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2010 48 685-692 Study of conformations and hydrogen bonds in the configurational isomers of pyrrole-2-carbaldehyde oxime by 1H, 13C and 15N NMR spectroscopy combined with MP2 and DFT calculations and NBO analysis (pages 685¨C692) Andrei V. Afonin, Igor A. Ushakov, Dmitry V. Pavlov, Andrei V. Ivanov and Al'bina I. Mikhaleva Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound (Z)-7 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2009 47 879-884 Pronounced stereospecificity of 1H, 13C, 15N and 77Se shielding constants in the selenophenyl oximes as shown by NMR spectroscopy and GIAO calculations (pages 879¨C884) Andrei V. Afonin, Dmitry V. Pavlov, Igor A. Ushakov, Elena Yu. Schmidt and Al'bina I. Mikhaleva Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . alkaloid ÏàËÆ¶È:66.6% Tetrahedron Letters 1987 28 163-164 Salvadoricine - a new indole alkaloid from the leaves of Salvadora persica Sohail Malik, Syed Salman Ahmad, Syed Imtiaz Haider, Anjum Muzaffar Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-(4-bromophenyl)-1H-pyrrole C10H8BrN ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2010 3621-3630 C¨CN Bond Formation Catalysed by CuI Bonded to Polyaniline Nanofiber Racha Arundhathi, Desitti Chaitanya Kumar and Bojja Sreedhar Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . N-phenyl pyrrole ÏàËÆ¶È:66.6% Tetrahedron 2013 69 1038-1042 Cooperatively assisted N-arylation using organic ionic base¨CBrønsted acid combination under controlled microwave heating Rahul Singh, Bharat Kumar Allam, Dushyant Singh Raghuvanshi, Krishna Nand Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 1f ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1988 26 134-151 Effect of N-substituents on the 13C NMR parameters of azoles Mikael Begtrup, Jos¨¦ Elguero, Robert Faure, Pelayo Camps, Carmen Estop¨¢, Dušan Ilavsky, Alain Fruchier, Claude Marzin and Javier de Mendoza Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 10a ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1988 26 134-151 Effect of N-substituents on the 13C NMR parameters of azoles Mikael Begtrup, Jos¨¦ Elguero, Robert Faure, Pelayo Camps, Carmen Estop¨¢, Dušan Ilavsky, Alain Fruchier, Claude Marzin and Javier de Mendoza Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 17n ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1988 26 134-151 Effect of N-substituents on the 13C NMR parameters of azoles Mikael Begtrup, Jos¨¦ Elguero, Robert Faure, Pelayo Camps, Carmen Estop¨¢, Dušan Ilavsky, Alain Fruchier, Claude Marzin and Javier de Mendoza Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ortho-substituted anisole(X=NCOCH3) ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1989 27 158-161 Experimental and theoretical study of the methoxy group conformational effect on 13C chemical shifts in ortho-substituted anisoles Rodolfo R. Biekofsky, Alicia B. Pomilio, Ruben H. Econteras, Dora G. de Kowalewski and Julio C. Facelli Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ortho-substituted anisole(X=NCOCH3) ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1989 27 158-161 Experimental and theoretical study of the methoxy group conformational effect on 13C chemical shifts in ortho-substituted anisoles Rodolfo R. Biekofsky, Alicia B. Pomilio, Ruben H. Econteras, Dora G. de Kowalewski and Julio C. Facelli Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 1k C10H9N ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2000 37 15-24 Synthesis and nuclear magnetic resonance spectroscopic studies of 1-arylpyrroles Chang Kiu Lee, Jung Ho Jun and Ji Sook Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 2,5-bis(N-carbazolyl)thiophene C28H18N2S ÏàËÆ¶È:62.5% Heterocycles 2009 78 1265-1269 Substituent Effects on Photophysical Properties of N-Thienylcarbazoles Hideyuki Shimizu, Atsushi Kobayashi, Shingo Itoi, Toshitada Yoshihara, Seiji Tobita, Yosuke Nakamura, and Jun Nishimura Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-05 12:13:43














»Ø¸´´ËÂ¥