2,9-Dichloro-1,10-phenanthroline.

Clicks: 471
ID: 67569
2009
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Article Quality & Performance Metrics
Overall Quality Improving Quality
57.8 /100
Combines engagement data with AI-assessed academic quality
AI Quality Assessment 🥈 High Quality
79.6 /100
Academic Rigor 90.0%
Novelty 70.0%
Clarity 88.0%
Key Strengths
  • Precise structural determination
  • Clear and concise writing
  • Focus on a specific molecule
Areas for Improvement
  • Limited context provided for the study's significance
  • Lack of discussion on potential applications
  • The novelty is somewhat limited, as it's a structural determination of a known compound.
AI Recommendations

The article could benefit from a brief discussion of the potential uses or properties of 2,9-Dichloro-1,10-phenanthroline. Adding context about why this specific molecule was chosen for study would also enhance the paper.

Enhanced v2.0 Analysis NISO/DORA Compliant
NISO/DORA Compliant
📊 Established
Topic Trend
2025 Relevance
Relevance
0%
Importance
0%
Authorship
Unknown
Authors
0
Diversity
0%
Research Integrity
COPE Standards
Integrity
0%
Innovation
0%
Interdisciplinary Value
↔️ Some cross-field connections
55%
Practical Impact Potential
Real-world Applications
60%
Enhanced Evaluation v2.0: Following NISO RP-25-2016, DORA 2025, and COPE assessment standards with 13 quality dimensions.
Readership in this journal
Emerging

Ranked #12 of 280 articles by views in acta crystallographica section e

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Abstract
The title mol-ecule, C(12)H(6)Cl(2)N(2), is almost planar (the r.m.s. deviation of C atoms is 0.04 Å). The C-N and C-C distances indicate delocalization of the π-electrons in the aromatic fused-ring system.
Reference Key
nadeem200929dichloro110phenanthrolineacta Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Nadeem, Said;Shah, Muhammad Raza;Ng, Seik Weng;
Journal acta crystallographica section e
Year 2009
DOI
10.1107/S1600536809011180
URL
http://scripts.iucr.org/cgi-bin/paper?S1600536809011180
Keywords
alkaline phosphatase aqueous liver injury hepatoprotective in vivo carbon tetrachloride ast alp alt ccl(4) dodonaea viscosa etoac h(2)o hautriwaic acid meoh alanine aminotransferase aspartate transaminase ethyl acetate methanolic extract

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